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Nature Methods
|
May 19, 2015
Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection
Adam D Ewing, Kathleen E Houlahan, Yin Hu, et al.
Biorxiv : the Preprint Server for Biology
|
September 18, 2025
Robust software development practices improve citations of RNA-seq tools
Sanskruti Sharma, Ecem Ilgun, Tuna Okcu, et al.
Arxiv
|
October 3, 2025
A decentralized future for the open-science databases
Gaurav Sharma, Viorel Munteanu, Nika Mansouri Ghiasi, et al.
STAR Protocols
|
March 19, 2025
Protocol for assessing distances in pathway space for classifier feature sets from machine learning methods
Bahar Tercan, Victor H Apolonio, Vinicius S Chagas, et al.
Nature Genetics
|
May 19, 2026
Towards a decentralized future for open-science databases
Gaurav Sharma, Viorel Munteanu, Nika Mansouri Ghiasi, et al.
Genome Biology
|
November 8, 2018
Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection
Anna Y Lee, Adam D Ewing, Kyle Ellrott, et al.
Cell Systems
|
June 19, 2021
A community challenge to evaluate RNA-seq, fusion detection, and isoform quantification methods for cancer discovery
Allison Creason, David Haan, Kristen Dang, et al.
Cell Genomics
|
February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space
Michael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
Nature Biotechnology
|
June 11, 2024
Crowd-sourced benchmarking of single-sample tumor subclonal reconstruction
Adriana Salcedo, Maxime Tarabichi, Alex Buchanan, et al.
Cancer Cell
|
January 3, 2025
Classification of non-TCGA cancer samples to TCGA molecular subtypes using compact feature sets
Kyle Ellrott, Christopher K Wong, Christina Yau, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
Nature Methods
|
May 19, 2015
Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection
Adam D Ewing, Kathleen E Houlahan, Yin Hu, et al.
Biorxiv : the Preprint Server for Biology
|
September 18, 2025
Robust software development practices improve citations of RNA-seq tools
Sanskruti Sharma, Ecem Ilgun, Tuna Okcu, et al.
Arxiv
|
October 3, 2025
A decentralized future for the open-science databases
Gaurav Sharma, Viorel Munteanu, Nika Mansouri Ghiasi, et al.
STAR Protocols
|
March 19, 2025
Protocol for assessing distances in pathway space for classifier feature sets from machine learning methods
Bahar Tercan, Victor H Apolonio, Vinicius S Chagas, et al.
Nature Genetics
|
May 19, 2026
Towards a decentralized future for open-science databases
Gaurav Sharma, Viorel Munteanu, Nika Mansouri Ghiasi, et al.
Genome Biology
|
November 8, 2018
Combining accurate tumor genome simulation with crowdsourcing to benchmark somatic structural variant detection
Anna Y Lee, Adam D Ewing, Kyle Ellrott, et al.
Cell Systems
|
June 19, 2021
A community challenge to evaluate RNA-seq, fusion detection, and isoform quantification methods for cancer discovery
Allison Creason, David Haan, Kristen Dang, et al.
Cell Genomics
|
February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space
Michael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
Nature Biotechnology
|
June 11, 2024
Crowd-sourced benchmarking of single-sample tumor subclonal reconstruction
Adriana Salcedo, Maxime Tarabichi, Alex Buchanan, et al.
Cancer Cell
|
January 3, 2025
Classification of non-TCGA cancer samples to TCGA molecular subtypes using compact feature sets
Kyle Ellrott, Christopher K Wong, Christina Yau, et al.
Page
of 6