Tag Archive

geoduck,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

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OA

Metabolic scaling bfactor

  • 1 min read

Objective and summary:


When possible, it is critical to normalize physiological rates allometrically, as they are often proportional to boy mass.

Read More

Argopecten Qubit 20220608

  • ~1 min read

Objective and summary:


  • DNA extractions of juvenile first generation Bay scalops (F1 A. irradians) extracted 12 indiviauls samples

Read More

Argopecten Qubit 20220131

  • 1 min read

Objective and summary:

  • Complete extraction and qubit quantification using non-target adult scallop samples

    • 30 mg and 90 mg of tissue
    • 3 hr Proteinase K incubation at 120 RPM and 55C - vortexed every hour
    • doubled the volume of TL Buffer, HBC buffer and 100% ethanol for the 60 mg samples (did not double proteinase K)

Read More

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

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scallop,

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

Read More

Argopecten Qubit 20220608

  • ~1 min read

Objective and summary:


  • DNA extractions of juvenile first generation Bay scalops (F1 A. irradians) extracted 12 indiviauls samples

Read More

Argopecten Qubit 20220131

  • 1 min read

Objective and summary:

  • Complete extraction and qubit quantification using non-target adult scallop samples

    • 30 mg and 90 mg of tissue
    • 3 hr Proteinase K incubation at 120 RPM and 55C - vortexed every hour
    • doubled the volume of TL Buffer, HBC buffer and 100% ethanol for the 60 mg samples (did not double proteinase K)

Read More

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DNA,

Argopecten Qubit 20220608

  • ~1 min read

Objective and summary:


  • DNA extractions of juvenile first generation Bay scalops (F1 A. irradians) extracted 12 indiviauls samples

Read More

F0 Aropecten Qubit 20220110

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Aropecten Qubit 20220105

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Argopecten Qubit 20220104

  • ~1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in late December 2021)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

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extractions,

Argopecten Qubit 20220608

  • ~1 min read

Objective and summary:


  • DNA extractions of juvenile first generation Bay scalops (F1 A. irradians) extracted 12 indiviauls samples

Read More

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zymo,

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Qubit,

Argopecten Qubit 20220608

  • ~1 min read

Objective and summary:


  • DNA extractions of juvenile first generation Bay scalops (F1 A. irradians) extracted 12 indiviauls samples

Read More

F0 Aropecten Qubit 20220110

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Aropecten Qubit 20220105

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Argopecten Qubit 20220104

  • ~1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in late December 2021)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

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NOAA

F0 Aropecten Qubit 20220110

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Aropecten Qubit 20220105

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Argopecten Qubit 20220104

  • ~1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in late December 2021)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

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RNA,

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DNA

Argopecten Qubit 20220131

  • 1 min read

Objective and summary:

  • Complete extraction and qubit quantification using non-target adult scallop samples

    • 30 mg and 90 mg of tissue
    • 3 hr Proteinase K incubation at 120 RPM and 55C - vortexed every hour
    • doubled the volume of TL Buffer, HBC buffer and 100% ethanol for the 60 mg samples (did not double proteinase K)

Read More

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scallops,

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

Read More

Scallop tagging

  • ~1 min read

Objective and summary:


  • Measure and tag all Bay scallops in the minnow cool systems. There are two sets of scallops that have been reared under raw water common garden from the 8 and 7.5 pH conditions.
    • March 6th (‘old’ group)
    • April 26th (‘new’ group)

Read More

F0 Aropecten Qubit 20220110

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Aropecten Qubit 20220105

  • 1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in early January 2022)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

F0 Argopecten Qubit 20220104

  • ~1 min read

Objective and summary:

  • Measure DNA concentrations of DNA extracted from F0 adult Bay scallop adductor tissue (dissected and extracted in late December 2021)
  • DNA was extracted using the OMEGA EZNA Tissue kit protocol here
  • Ran Qubit dsDNA BR kit following standard protocol thermosci online pdf

Read More

Back to Top ↑

Qubit

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dna,

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OA,

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

Read More

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

extractions

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prep,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

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rna

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extraction,

Argopecten Qubit 20220131

  • 1 min read

Objective and summary:

  • Complete extraction and qubit quantification using non-target adult scallop samples

    • 30 mg and 90 mg of tissue
    • 3 hr Proteinase K incubation at 120 RPM and 55C - vortexed every hour
    • doubled the volume of TL Buffer, HBC buffer and 100% ethanol for the 60 mg samples (did not double proteinase K)

Read More

Back to Top ↑

protocol

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

RNA

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experiment,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

qubit,

Argopecten Qubit 20220131

  • 1 min read

Objective and summary:

  • Complete extraction and qubit quantification using non-target adult scallop samples

    • 30 mg and 90 mg of tissue
    • 3 hr Proteinase K incubation at 120 RPM and 55C - vortexed every hour
    • doubled the volume of TL Buffer, HBC buffer and 100% ethanol for the 60 mg samples (did not double proteinase K)

Read More

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workshop

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rna,

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tagseq,

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gel,

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scallops

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scallop

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Illumina,

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Rclub

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protein,

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

Back to Top ↑

Geoduck,

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

2020,

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

stress

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

response,

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

hatchery,

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

heathstack,

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

Point

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

Whitney

Experiment Prep Point Whitney

  • 1 min read

read.me

The following is a summary of a trip to Jamestown Point Whitney Shellfish Hatchery in Brinnon, Washingston frmo 3/6/20 - 3/13/20.

Read More

Back to Top ↑

qPCR

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

blasp,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

blastn,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

Augustus,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

Muscle,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

Pfam,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

protein

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

NADH dehydrogenase Pgenerosa Identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein NADH dehydrogenase (complex I) This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

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design,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

Back to Top ↑

tagseq

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extraction

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TA,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

pH,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

APEX,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

sal,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

Back to Top ↑

research,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

Read More

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HISAT2,

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samtools,

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StringTie,

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fastqc,

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multiqc,

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fastp

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oyster,

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omega,

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hemolymph

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C6_plus

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oyster

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hemolymph,

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

Read More

Back to Top ↑

flow

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

Read More

Back to Top ↑

library

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growth,

Scallop tagging

  • ~1 min read

Objective and summary:


  • Measure and tag all Bay scallops in the minnow cool systems. There are two sets of scallops that have been reared under raw water common garden from the 8 and 7.5 pH conditions.
    • March 6th (‘old’ group)
    • April 26th (‘new’ group)

Read More

Back to Top ↑

Milford

Scallop tagging

  • ~1 min read

Objective and summary:


  • Measure and tag all Bay scallops in the minnow cool systems. There are two sets of scallops that have been reared under raw water common garden from the 8 and 7.5 pH conditions.
    • March 6th (‘old’ group)
    • April 26th (‘new’ group)

Read More

Back to Top ↑

respiration

Metabolic scaling bfactor

  • 1 min read

Objective and summary:


When possible, it is critical to normalize physiological rates allometrically, as they are often proportional to boy mass.

Read More

Back to Top ↑

metabolism

Metabolic scaling bfactor

  • 1 min read

Objective and summary:


When possible, it is critical to normalize physiological rates allometrically, as they are often proportional to boy mass.

Read More

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R

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markdown

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physiology,

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

Back to Top ↑

total

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

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antioxidant

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

Back to Top ↑

capacity

Phys Assays Pipeline

  • 6 min read

Pipeline for geoduck physiology (oxidative stress, total protein, & AFDW/condition index)

NOTE: the following protocol was followed in analysis of juvenile geoduck (~5-8mm shell length) from an OA experiment completed in summer 2019. Juvenile geoduck (whole animals) were snap frozen in LN2 at the hatcheryand stored at -80°C until later analysis

Read More

Back to Top ↑

qPCR,

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

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genome,

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

augustus,

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

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blastp,

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

Back to Top ↑

jalview

AOX Pgenerosa identification

  • 2 min read

OBJECTIVE

The following protocol was completed with the geoduck genome in preparation for primer design and qPCR of a target protein Alternative oxidase This step-by-step process can be used to verify the presence/absence of a particular target gene within an annotated genome without gene family identification. In this case.. a database of the geoduck genome was used with only ID identifiers for genes (no family-specific accession ID)

Read More

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primer,

Primer Design

  • 8 min read

Read.me

The following is a condensed summary of computational work from blast gene identification to primer testing in preparation for qPCR.

Read More

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geoduck

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proteins

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blast

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histology

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overview,

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coral,

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porites,

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lab

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meeting,

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trininty,

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trinotate,

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busco

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metabolomics,

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Rutgers,

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metabolomics

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ANOVA,

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histology,

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gonad,

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gametogenesis

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extrations,

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tem,

Daily Wet Lab OA at Point Whitney

  • 12 min read

Point Whitney Hatchery and Lab Information

Last Revised: 20181030 SJ Gurr

Lab Need to Know:
  • Dry bench (1st bench, closest to light set switches) should stay dry, do not move wet/liquid materials since electronics including laptops are kept here.

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dna,rna

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zymop,

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qc,

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dyna,

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repeated

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ut,

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library,

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quality,

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temperature,

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O2

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sensor,

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dissolved

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oxygen,

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Tagseq,

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fastp,

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mutliqc,

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trimming,

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polyA

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tail,

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low

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complexity

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filtering

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DESeq2,

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TagSeq,

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mRNA,

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differential

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expression,

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stats,

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model

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multivariate

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NOAA,

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postdoc

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gels,

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electrophoresis,

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lab,

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benchtop

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JC-10

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DCFHDA

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SYBR_green

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Extractions,

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crassostrea,

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cytometry,

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C6

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plus,

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BD

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biosciences

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Crassostrea

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flow_cytometry,

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library_prep

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Illumina

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gel_electrophoresis

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common

Scallop tagging

  • ~1 min read

Objective and summary:


  • Measure and tag all Bay scallops in the minnow cool systems. There are two sets of scallops that have been reared under raw water common garden from the 8 and 7.5 pH conditions.
    • March 6th (‘old’ group)
    • April 26th (‘new’ group)

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garden,

Scallop tagging

  • ~1 min read

Objective and summary:


  • Measure and tag all Bay scallops in the minnow cool systems. There are two sets of scallops that have been reared under raw water common garden from the 8 and 7.5 pH conditions.
    • March 6th (‘old’ group)
    • April 26th (‘new’ group)

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raw

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data,

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basespace,

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command

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line,

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spawners

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RShiny,

RShiny calculator app (algae feed)

  • 3 min read

How to build an RShiny - algae feed calculator:


Showcase an simple example of an RShiny built for calculating the volume of known algae culture for feeding bivalve larvae

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application,

RShiny calculator app (algae feed)

  • 3 min read

How to build an RShiny - algae feed calculator:


Showcase an simple example of an RShiny built for calculating the volume of known algae culture for feeding bivalve larvae

Read More

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algae,

RShiny calculator app (algae feed)

  • 3 min read

How to build an RShiny - algae feed calculator:


Showcase an simple example of an RShiny built for calculating the volume of known algae culture for feeding bivalve larvae

Read More

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efficiency,

RShiny calculator app (algae feed)

  • 3 min read

How to build an RShiny - algae feed calculator:


Showcase an simple example of an RShiny built for calculating the volume of known algae culture for feeding bivalve larvae

Read More

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R,

RShiny calculator app (algae feed)

  • 3 min read

How to build an RShiny - algae feed calculator:


Showcase an simple example of an RShiny built for calculating the volume of known algae culture for feeding bivalve larvae

Read More

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Milford,

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

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feed,

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

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larvae,

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

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static

SOP Feeding larvae

  • 6 min read

SOP! Feeding larvae in static system


Objective:

Batch feed larvae using all precautions necessary for a static system (1) assess the current algal density of both the culture and static larval system using flow cytometry (2) add the correct volume of algae to a target cell density.

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JC10,

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

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bay

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

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SYBR

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

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green,

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

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gating,

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

Read More

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cytometry

Hemolymph Bay scallop (testing)

  • 1 min read

Objective:

Bleed a few extra scallops (hatchery in the basement) from the F1 common garden culls ealier this year. Test SYBR green and JC-10 in hemolymph using the protocol written earlier this year with results summarized here

Read More

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bfactor

Metabolic scaling bfactor

  • 1 min read

Objective and summary:


When possible, it is critical to normalize physiological rates allometrically, as they are often proportional to boy mass.

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scaling

Metabolic scaling bfactor

  • 1 min read

Objective and summary:


When possible, it is critical to normalize physiological rates allometrically, as they are often proportional to boy mass.

Read More

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citation

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zenodo

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Rmarkdown

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git

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github

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RClub

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Presens

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Loligo

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lcWGS

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workflow

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pipeline

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if

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else

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boolean

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forloop

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aquaculture,

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handbook,

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priming

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