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Updated manuscript: add D3b/DBHI authors to date #107

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jharenza opened this issue Jul 9, 2020 · 29 comments
Closed

Updated manuscript: add D3b/DBHI authors to date #107

jharenza opened this issue Jul 9, 2020 · 29 comments
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@jharenza
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jharenza commented Jul 9, 2020

What section of the manuscript should be updated?

Author list

Proposed changes

This issue is being opened to track D3b authors and roles for the OpenPBTA manuscript.

Relevant literature

We will use CRediT taxonomy. Alternate link.

Below, we will add full author names for the roles below and then file a PR:

Role Authors
Conceptualization Jo Lynne Rokita, Pichai Raman, Adam C. Resnick, Jena V. Lily, Philip B. Storm
Data curation Jo Lynne Rokita, Krutika S. Gaonkar, Yuankun Zhu, Miguel A. Brown, Brian M. Ennis, Bo Zhang, Bailey Farrow, Nick VanKuren, Payal Jain
Formal Analysis Jo Lynne Rokita, Krutika S. Gaonkar, Yuankun Zhu, Tejaswi Koganti, Shrivats Kannan, Nhat Duong, Komal S. Rathi, Pichai Raman, Daniel P. Miller, Mateusz P. Koptyra, Miguel A. Brown, Bo Zhang, Brian M. Ennis
Funding acquisition Adam C. Resnick, Philip B. Storm, Jo Lynne Rokita, Jena V. Lilly
Investigation Jo Lynne Rokita, Krutika S. Gaonkar, Nhat Duong, Komal S. Rathi, Yuankun Zhu, Tejaswi Koganti, Mariarita Santi, Angela Viaene, Miguel A. Brown, Payal Jain
Methodology Jo Lynne Rokita, Krutika S. Gaonkar, Shrivats Kannan, Nhat Duong, Hongbo M. Xie, Komal S. Rathi, Pichai Raman, Yuankun Zhu, Miguel A. Brown, Adam A. Kraya
Project administration Jena V. Lilly, Allison P. Heath
Resources Adam C. Resnick, Philip B. Storm
Software Jo Lynne Rokita, Krutika S. Gaonkar, Bailey Farrow, Nick VanKuren
Supervision Adam C. Resnick, Yuankun Zhu, Jo Lynne Rokita, Angela Waanders, Hongbo M. Xie, Cassie N. Kline
Validation Mariarita Santi, Angela Viaene, Derek Hanson, Payal Jain
Visualization
Writing – original draft Jo Lynne Rokita, Krutika S. Gaonkar, Shrivats Kannan, Komal S. Rathi, Miguel A. Brown, Jessica Wong, Mateusz P. Koptyra
Writing – review & editing

Collecting ORCIDs here.

@jharenza jharenza self-assigned this Jul 9, 2020
@jharenza
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jharenza commented Jul 9, 2020

cc @yuankunzhu, @allisonheath, @baileyckelly, @tatianapatton to add people from your teams

@jharenza jharenza changed the title Updated manuscript: add D3b authors to date Updated manuscript: add D3b/DBHI authors to date Jul 9, 2020
@yuankunzhu
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@jharenza, I think we can add

@jharenza
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jharenza commented Jul 10, 2020

@yuankunzhu, thanks, done. Also, think about the data processing (I think "Formal Analysis") for releases - I know Brian worked on a lot of that - what about Bo? I will also add Miguel for CNV algorithms (and possibly David for Theta2 calculations?).

@jharenza
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also cc @mkoptyra for your roles

@aadamk
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aadamk commented Jul 13, 2020

Below are my contributions for authorship:

  1. 'Supervision' for work related to the development and oversight of the analysis toolkit
  2. 'Methodology' for development of a new TMB protocol (@tkoganti can be added under this section for implementation of the 'Friends of Cancer Research' harmonization standards)
  3. 'Methodology' for development of a standardized RNAseq batch correction methodology (with @komalsrathi, though she is already listed under 'methodology'; soon to be merged to d3b-analysis-toolkit repo).

@komalsrathi
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@jaclyn-taroni am I correct in saying that we did not combine the polya + stranded samples for any OpenPBTA analyses? If so, @aadamk we don't need to use the batch correction methodology for the OpenPBTA manuscript. So, you can remove (3) from above.

@jaclyn-taroni
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@komalsrathi Yes that is correct, we do not use any combined poly-A and ribodeplete manuscript in this project currently.

@aadamk
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aadamk commented Jul 13, 2020

I see.
As I understood, D3b was looking to merge modularized code for different DNA + RNA analyses. My thoughts were that this would include @komalsrathi's batch correction module to enable researchers to batch correct on the basis of site, as PBTA is inclusive of CBTTC + PNOC003 (and possibly 008 samples) in this release.
Though do correct me if I am mistaken.

@jaclyn-taroni
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There is no pull request to include the batch correction module as of yet.

As I understood, D3b was looking to merge modularized code for different DNA + RNA analyses.

Can someone from D3b file an issue on https://github.com/AlexsLemonade/OpenPBTA-analysis so we have an idea of what to expect please? I think that will help us all get on the same page.

@komalsrathi
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@yuankunzhu please clarify if there are any plans for the above and if there has been any correspondence with CCDL about incorporating one or more modules from the D3b toolkit.

@mkoptyra
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Below are my contributions for authorship:

  1. Formal Analysis - Molecularly subtype chordomas
  2. Writing - Methods sections: Biospecimen collection and Nucleic acids extraction and library preparation

@yuankunzhu
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@yuankunzhu please clarify if there are any plans for the above and if there has been any correspondence with CCDL about incorporating one or more modules from the D3b toolkit.

I think the plan is to use the current data release and existing analyses to prepare the manuscript, while for other modules and tools, we can bring them in after the manuscript drafting and keep iterating from there. That's my take away from our recent OpenPBTA call, but wanted to check if that's a shared understanding @jaclyn-taroni @jharenza @aadamk 🙂.

@jharenza
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@yuankunzhu please clarify if there are any plans for the above and if there has been any correspondence with CCDL about incorporating one or more modules from the D3b toolkit.

I think the plan is to use the current data release and existing analyses to prepare the manuscript, while for other modules and tools, we can bring them in after the manuscript drafting and keep iterating from there. That's my take away from our recent OpenPBTA call, but wanted to check if that's a shared understanding @jaclyn-taroni @jharenza @aadamk 🙂.

I think that's right. @aadamk, I added you to Methodology for now, since that is definitely being used for V1 of the paper, and if we add the modules/batch correction, we can add those contributions later.

@aadamk
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aadamk commented Jul 14, 2020

Got it - makes sense @yuankunzhu and @jharenza. Thanks!

@jharenza
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jharenza commented Jul 15, 2020

Tracking authorship contributions in more detail here:

Jo Lynne Rokita (@jharenza)

  • Conceptualization - conceiving open analysis via GitHub
  • Data curation - pbta-histologies.tsv V1-V15, data releases
  • Formal analysis - run initial GISTIC analysis
  • Funding acquisition - ALSF Catalyst Award
  • Investigation - ControlFreeC and CNVKit copy number algorithm benchmarking, ploidy analysis, QC histologies file/matrices, decision-making for fusion analysis module
  • Methodology - generate rules for molecular subtyping tickets, fusion analysis methods
  • Software - annoFuse as basis for fusion filtering and prioritization
  • Supervision - oversee D3b sprints to achieve upstream processing tasks and data releases, oversee fusion analysis/molecular subtyping
  • Writing – original draft - methods PRs

Krutika S. Gaonkar (@kgaonkar6)

Pichai Raman (@PichaiRaman)

  • Conceptualization - created many of the initial analysis request tickets
  • Formal Analysis - first iteration of ssGSEA
  • Methodology - create initial merge matrices for RNA-Seq data

Komal S. Rathi (@komalsrathi

Shrivats Kannan (@shrivatsk)

@jharenza
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jharenza commented Jul 15, 2020

Nhat Duong (@fingerfen)

  • Formal Analysis - Copy number consensus
  • Investigation - related to CNV consensus
  • Methodology - generated method for CNV consensus

Hongbo M. Xie (@xiehongbo)

  • Methodology - generated method for CNV consensus
  • Supervision - of @fingerfen

Mariarita Santi and Angela Viaene

Teja Koganti (@tkoganti) - please let me know your full name for publication

  • Data curation - generation of merge matrices for data releases
  • Formal Analysis - TMB analysis, EPN subtyping
  • Investigation - investigation of TMB

Adding additional contributions:
Miguel A. Brown (@migbro)

  • Data curation - generation of merge matrices for data releases
  • Formal analysis - MendQC, ControlFreeC, CNVKit, Vardict, Lancet, Strelka2, Mutect2
  • Investigation - benchmarking of variant callers, CNV callers
  • Methodology - generating best practice workflows for above
  • Writing – original draft - methods

Brian M. Ennis (@bmennis)

  • Data curation - generation of merge matrices for data releases
  • Formal analysis - initial LUMPY analysis, Manta SV (?) - please confirm

Bo Zhang (@zhangb1)

  • Data curation - generation of merge matrices for data releases
  • Formal analysis - STAR, STAR-Fusion, Arriba analyses

@baileyckelly
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Bailey Farrow & Nick VanKuren

  • Data Curation
  • Software

@jharenza
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Derek Hanson (D3b collaborator)

@jharenza
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@fingerfen, will you please add your email to this google doc for authorship purposes? thanks!

@allisonheath
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Allison P. Heath

  • Project administration

@jharenza jharenza mentioned this issue Aug 14, 2020
5 tasks
@jainpayal022
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Thanks @jharenza, on my end it will be the following:

  1. Data curation - Compiled and collated PNOC003-related data along with supervising WGS data generation.
  2. Validation - of fusion related output from annoFuse, LGG and HGG domain specific knowledge contribution
  3. Investigation - QC of manifest building clinical and histologies file for V16/V17
  4. Writing – review & editing of next manuscript iteration

@jharenza
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Thanks @jharenza, on my end it will be the following:

  1. Data curation - Compiled and collated PNOC003-related data along with supervising WGS data generation.
  2. Validation - of fusion related output from annoFuse, LGG and HGG domain specific knowledge contribution
  3. Investigation - QC of manifest building clinical and histologies file for V16/V17
  4. Writing – review & editing of next manuscript iteration

Thanks @jainpayal022 - I will leave off 4 right now, as I had noted those who had already written some pieces. We can add this contribution later.

jharenza pushed a commit that referenced this issue Aug 14, 2020
add author contributions as noted [here](#107) and added payal as author
@syzheng
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syzheng commented Sep 1, 2020

@jharenza @jaclyn-taroni @NNoureen
For us,
Data analysis - telomerase activity prediction.
writing - contributing the corresponding method description.

@jaclyn-taroni
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@syzheng can you add your contributions, affiliations, and contact info to #115 and use the specific roles from CRediT when you do please? The available roles are (link to the definitions is included on #115):

Conceptualization
Data curation
Formal Analysis
Funding acquisition
Investigation
Methodology
Project administration
Resources
Software
Supervision
Validation
Visualization
Writing – original draft
Writing – review & editing

@syzheng
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syzheng commented Sep 1, 2020

@jaclyn-taroni @NNoureen
Sure.
Contribution:
Formal Analysis: we contributed telomerase activity analysis
Writing – Original Draft: we contributed description of telomerase prediction methods and made figures to show distribution of telomerase activity across disease entities.

Affiliations:
Greehey Children's Cancer Research Institute, UT Health San Antonio

Contact info:
Siyuan Zheng
Initial - Z.S.
Email - zhengs3@uthscsa.edu
Twitter - @zhengsiyuan
ORCID - 0000-0002-1031-9424

@NNoureen please provide your contact info.

@NNoureen
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NNoureen commented Sep 1, 2020

@jaclyn-taroni @syzheng

Affiliations:
Greehey Children's Cancer Research Institute, UT Health San Antonio

Contact info:
Nighat Noureen
Initial: N.N.
Email: noureen@uthscsa.edu
ORCID: 0000-0001-7495-8201

@jharenza
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Cassie N. Kline

  • Supervision - informing CNS_region in V17 `pbta-histologies.tsv
  • Validation of histologies nomenclature

@jharenza
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Angela Waanders

  • Supervision - informing HGG subtyping, glioma_brain_region, and overall histology nomenclature

@jharenza
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closed with #111 and #122

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