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Trends in Genetics : TIG
|
May 21, 2013
Properties and rates of germline mutations in humans
Catarina D Campbell, Evan E Eichler
Annual Review of Genetics
|
August 23, 2011
Human copy number variation and complex genetic disease
Santhosh Girirajan, Catarina D Campbell, Evan E Eichler
Genome Research
|
February 8, 2008
A survey of allelic imbalance in F1 mice
Catarina D Campbell, Andrew Kirby, James Nemesh, et al.
BMC Cancer
|
June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptome
Bernard Pereira, Emma Labrot, Eric Durand, et al.
Genome Biology
|
October 31, 2025
Natural language processing of gene descriptions for overrepresentation analysis with GeneTEA
Isabella A Boyle, Nayeem Akram Aquib, Mustafa Kocak, et al.
Source Code for Biology and Medicine
|
December 22, 2016
PureCN: copy number calling and SNV classification using targeted short read sequencing
Markus Riester, Angad P Singh, A Rose Brannon, et al.
Genome Biology
|
July 19, 2024
A benchmark of computational methods for correcting biases of established and unknown origin in CRISPR-Cas9 screening data
Alessandro Vinceti, Raffaele M Iannuzzi, Isabella Boyle, et al.
Science Translational Medicine
|
March 29, 2023
Clonal hematopoiesis detection in patients with cancer using cell-free DNA sequencing
Lauren Fairchild, Jeanne Whalen, Katie D'Aco, et al.
Ejhaem
|
August 21, 2023
Next-generation sequencing of baseline genetic mutations and outcomes of eltrombopag and azacitidine therapy in patients with myelodysplastic syndromes and thrombocytopenia: Data from the SUPPORT clinical trial
Pedro Marques Ramos, Jeea Choi, Catarina D Campbell, et al.
Nature Genetics
|
July 26, 2005
Demonstrating stratification in a European American population
Catarina D Campbell, Elizabeth L Ogburn, Kathryn L Lunetta, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Trends in Genetics : TIG
|
May 21, 2013
Properties and rates of germline mutations in humans
Catarina D Campbell, Evan E Eichler
Annual Review of Genetics
|
August 23, 2011
Human copy number variation and complex genetic disease
Santhosh Girirajan, Catarina D Campbell, Evan E Eichler
Genome Research
|
February 8, 2008
A survey of allelic imbalance in F1 mice
Catarina D Campbell, Andrew Kirby, James Nemesh, et al.
BMC Cancer
|
June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptome
Bernard Pereira, Emma Labrot, Eric Durand, et al.
Genome Biology
|
October 31, 2025
Natural language processing of gene descriptions for overrepresentation analysis with GeneTEA
Isabella A Boyle, Nayeem Akram Aquib, Mustafa Kocak, et al.
Source Code for Biology and Medicine
|
December 22, 2016
PureCN: copy number calling and SNV classification using targeted short read sequencing
Markus Riester, Angad P Singh, A Rose Brannon, et al.
Genome Biology
|
July 19, 2024
A benchmark of computational methods for correcting biases of established and unknown origin in CRISPR-Cas9 screening data
Alessandro Vinceti, Raffaele M Iannuzzi, Isabella Boyle, et al.
Science Translational Medicine
|
March 29, 2023
Clonal hematopoiesis detection in patients with cancer using cell-free DNA sequencing
Lauren Fairchild, Jeanne Whalen, Katie D'Aco, et al.
Ejhaem
|
August 21, 2023
Next-generation sequencing of baseline genetic mutations and outcomes of eltrombopag and azacitidine therapy in patients with myelodysplastic syndromes and thrombocytopenia: Data from the SUPPORT clinical trial
Pedro Marques Ramos, Jeea Choi, Catarina D Campbell, et al.
Nature Genetics
|
July 26, 2005
Demonstrating stratification in a European American population
Catarina D Campbell, Elizabeth L Ogburn, Kathryn L Lunetta, et al.
Page
of 4