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Bioinformatics (Oxford, England)
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March 20, 2018
Integrating long-range connectivity information into de Bruijn graphs
Isaac Turner, Kiran V Garimella, Zamin Iqbal, et al.
Bioinformatics (Oxford, England)
|
January 3, 2025
Fast and exact gap-affine partial order alignment with POASTA
Lucas R van Dijk, Abigail L Manson, Ashlee M Earl, et al.
Genome Biology and Evolution
|
August 5, 2022
A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos)
Ellie E Armstrong, Blair W Perry, Yongqing Huang, et al.
Genome Research
|
August 21, 2020
Detection of simple and complex de novo mutations with multiple reference sequences
Kiran V Garimella, Zamin Iqbal, Michael A Krause, et al.
European Journal of Human Genetics : EJHG
|
November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing data
Laurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
Current Protocols in Bioinformatics
|
November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Nature Communications
|
January 3, 2024
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
Livius Penter, Mehdi Borji, Adi Nagler, et al.
Nature Genetics
|
June 14, 2011
Variation in genome-wide mutation rates within and between human families
Donald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Nature Biotechnology
|
June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenation
Aziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Nature Genetics
|
April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A DePristo, Eric Banks, Ryan Poplin, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
March 20, 2018
Integrating long-range connectivity information into de Bruijn graphs
Isaac Turner, Kiran V Garimella, Zamin Iqbal, et al.
Bioinformatics (Oxford, England)
|
January 3, 2025
Fast and exact gap-affine partial order alignment with POASTA
Lucas R van Dijk, Abigail L Manson, Ashlee M Earl, et al.
Genome Biology and Evolution
|
August 5, 2022
A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos)
Ellie E Armstrong, Blair W Perry, Yongqing Huang, et al.
Genome Research
|
August 21, 2020
Detection of simple and complex de novo mutations with multiple reference sequences
Kiran V Garimella, Zamin Iqbal, Michael A Krause, et al.
European Journal of Human Genetics : EJHG
|
November 24, 2016
A framework for the detection of de novo mutations in family-based sequencing data
Laurent C Francioli, Mircea Cretu-Stancu, Kiran V Garimella, et al.
Current Protocols in Bioinformatics
|
November 29, 2014
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline
Geraldine A Van der Auwera, Mauricio O Carneiro, Christopher Hartl, et al.
Nature Communications
|
January 3, 2024
Integrative genotyping of cancer and immune phenotypes by long-read sequencing
Livius Penter, Mehdi Borji, Adi Nagler, et al.
Nature Genetics
|
June 14, 2011
Variation in genome-wide mutation rates within and between human families
Donald F Conrad, Jonathan E M Keebler, Mark A DePristo, et al.
Nature Biotechnology
|
June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenation
Aziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Nature Genetics
|
April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A DePristo, Eric Banks, Ryan Poplin, et al.
Page
of 2