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Petr Danecek

Showing results (11-20 of 50) with videos related to

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Gigascience|February 17, 2021
HTSlib: C library for reading/writing high-throughput sequencing dataJames K Bonfield, John Marshall, Petr Danecek, et al.
Genetics in Medicine Open|December 13, 2024
Detection and characterization of copy-number variants from exome sequencing in the DDD studyPetr Danecek, Eugene J Gardner, Tomas W Fitzgerald, et al.
Genome Biology|April 25, 2012
High levels of RNA-editing site conservation amongst 15 laboratory mouse strainsPetr Danecek, Christoffer Nellåker, Rebecca E McIntyre, et al.
Gigascience|February 16, 2021
Twelve years of SAMtools and BCFtoolsPetr Danecek, James K Bonfield, Jennifer Liddle, et al.
Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.
Nature Genetics|October 4, 2016
Reference-based phasing using the Haplotype Reference Consortium panelPo-Ru Loh, Petr Danecek, Pier Francesco Palamara, et al.
Nature Genetics|August 11, 2022
Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cellsFoad J Rouhani, Xueqing Zou, Petr Danecek, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature Methods|March 24, 2020
Cardelino: computational integration of somatic clonal substructure and single-cell transcriptomesDavis J McCarthy, Raghd Rostom, Yuanhua Huang, et al.
Nature Communications|February 17, 2026
Author Correction: Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Gigascience|February 17, 2021
HTSlib: C library for reading/writing high-throughput sequencing dataJames K Bonfield, John Marshall, Petr Danecek, et al.
Genetics in Medicine Open|December 13, 2024
Detection and characterization of copy-number variants from exome sequencing in the DDD studyPetr Danecek, Eugene J Gardner, Tomas W Fitzgerald, et al.
Genome Biology|April 25, 2012
High levels of RNA-editing site conservation amongst 15 laboratory mouse strainsPetr Danecek, Christoffer Nellåker, Rebecca E McIntyre, et al.
Gigascience|February 16, 2021
Twelve years of SAMtools and BCFtoolsPetr Danecek, James K Bonfield, Jennifer Liddle, et al.
Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.
Nature Genetics|October 4, 2016
Reference-based phasing using the Haplotype Reference Consortium panelPo-Ru Loh, Petr Danecek, Pier Francesco Palamara, et al.
Nature Genetics|August 11, 2022
Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cellsFoad J Rouhani, Xueqing Zou, Petr Danecek, et al.
Nature Communications|November 3, 2025
Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Nature Methods|March 24, 2020
Cardelino: computational integration of somatic clonal substructure and single-cell transcriptomesDavis J McCarthy, Raghd Rostom, Yuanhua Huang, et al.
Nature Communications|February 17, 2026
Author Correction: Complex de novo structural variants are an underestimated cause of rare disordersHyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
Pageof 5