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Plos Computational Biology
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June 21, 2021
lra: A long read aligner for sequences and contigs
Jingwen Ren, Mark J P Chaisson
Nature Genetics
|
February 16, 2026
Author Correction: Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes
Walfred Ma, Mark J P Chaisson
Nature Genetics
|
October 17, 2025
Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes
Walfred Ma, Mark J P Chaisson
Genome Biology
|
May 7, 2022
TT-Mars: structural variants assessment based on haplotype-resolved assemblies
Jianzhi Yang, Mark J P Chaisson
Nature Communications
|
July 13, 2021
Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs
Tsung-Yu Lu, , Mark J P Chaisson
Genome Biology
|
July 27, 2023
vamos: variable-number tandem repeats annotation using efficient motif sets
Jingwen Ren, Bida Gu, Mark J P Chaisson
Nature Reviews. Genetics
|
October 8, 2015
Genetic variation and the de novo assembly of human genomes
Mark J P Chaisson, Richard K Wilson, Evan E Eichler
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
HQAlign: Aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
Arxiv
|
January 30, 2023
HQAlign: Aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
Bioinformatics (Oxford, England)
|
September 22, 2023
HQAlign: aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
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Search research articles
Search
Showing results (1-10 of 42) with videos related to
Sort By:
Page
of 5
Plos Computational Biology
|
June 21, 2021
lra: A long read aligner for sequences and contigs
Jingwen Ren, Mark J P Chaisson
Nature Genetics
|
February 16, 2026
Author Correction: Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes
Walfred Ma, Mark J P Chaisson
Nature Genetics
|
October 17, 2025
Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes
Walfred Ma, Mark J P Chaisson
Genome Biology
|
May 7, 2022
TT-Mars: structural variants assessment based on haplotype-resolved assemblies
Jianzhi Yang, Mark J P Chaisson
Nature Communications
|
July 13, 2021
Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs
Tsung-Yu Lu, , Mark J P Chaisson
Genome Biology
|
July 27, 2023
vamos: variable-number tandem repeats annotation using efficient motif sets
Jingwen Ren, Bida Gu, Mark J P Chaisson
Nature Reviews. Genetics
|
October 8, 2015
Genetic variation and the de novo assembly of human genomes
Mark J P Chaisson, Richard K Wilson, Evan E Eichler
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
HQAlign: Aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
Arxiv
|
January 30, 2023
HQAlign: Aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
Bioinformatics (Oxford, England)
|
September 22, 2023
HQAlign: aligning nanopore reads for SV detection using current-level modeling
Dhaivat Joshi, Suhas Diggavi, Mark J P Chaisson, et al.
Page
of 5