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Catarina D Campbell

Showing results (1-10 of 32) with videos related to

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Trends in Genetics : TIG|May 21, 2013
Properties and rates of germline mutations in humansCatarina D Campbell, Evan E Eichler
Annual Review of Genetics|August 23, 2011
Human copy number variation and complex genetic diseaseSanthosh Girirajan, Catarina D Campbell, Evan E Eichler
Genome Research|February 8, 2008
A survey of allelic imbalance in F1 miceCatarina D Campbell, Andrew Kirby, James Nemesh, et al.
BMC Cancer|June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptomeBernard Pereira, Emma Labrot, Eric Durand, et al.
Genome Biology|October 31, 2025
Natural language processing of gene descriptions for overrepresentation analysis with GeneTEAIsabella 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 sequencingMarkus 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 dataAlessandro 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 sequencingLauren 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 trialPedro Marques Ramos, Jeea Choi, Catarina D Campbell, et al.
Nature Genetics|July 26, 2005
Demonstrating stratification in a European American populationCatarina D Campbell, Elizabeth L Ogburn, Kathryn L Lunetta, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Trends in Genetics : TIG|May 21, 2013
Properties and rates of germline mutations in humansCatarina D Campbell, Evan E Eichler
Annual Review of Genetics|August 23, 2011
Human copy number variation and complex genetic diseaseSanthosh Girirajan, Catarina D Campbell, Evan E Eichler
Genome Research|February 8, 2008
A survey of allelic imbalance in F1 miceCatarina D Campbell, Andrew Kirby, James Nemesh, et al.
BMC Cancer|June 20, 2022
Contribution and clinical relevance of germline variation to the cancer transcriptomeBernard Pereira, Emma Labrot, Eric Durand, et al.
Genome Biology|October 31, 2025
Natural language processing of gene descriptions for overrepresentation analysis with GeneTEAIsabella 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 sequencingMarkus 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 dataAlessandro 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 sequencingLauren 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 trialPedro Marques Ramos, Jeea Choi, Catarina D Campbell, et al.
Nature Genetics|July 26, 2005
Demonstrating stratification in a European American populationCatarina D Campbell, Elizabeth L Ogburn, Kathryn L Lunetta, et al.
Pageof 4