Supplementary data including code for an science article 'Gaps and complex structurally variant loci in phased genome assemblies'
<p>The gene distribution of the 446 identified variants in the mtDNA genomes.</p
BACKGROUND: The last two human genome assemblies have extended the previous linear golden-path parad...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Overlap of public genomic tracks with genome assembly gaps of hg19 and hg38. Overlap of public genom...
<p>Details of discordant variants from whole genome and exome sequencing data.</p
Additional file 3. Chromosome-level assemblies from diverse clades reveal limited structural and gen...
<p>Gaps in the genome of isolate 70-15 filled with sequences from the field isolates P131 and/or Y34...
This repository contains code used in data processing, quality control, analysis and visualisation p...
This repository contains code used in - Data quality check and pre-GWAS prep Genome-wide associa...
This is an archived version of a code repository (https://bitbucket.org/4dnucleome/spatial_chromatin...
The uploaded file contains Supplementary Tables S1-S61 for the manuscript "Assembly of 43 human Y ch...
Supplemental data and code related to the manuscript: "Multifactorial heterogeneity of the huma...
Supplemental Material for Prevalence of chromosomal abnormalities identified by copy number variatio...
Statistics of variant analysis in heterozygous sites in genome of CBS 11270 and between genomes of C...
<p>Exome sequence variants shared by all affected individuals in homozygous or compound heterozygous...
<p>The gene distribution of the 446 identified variants in the mtDNA genomes.</p
BACKGROUND: The last two human genome assemblies have extended the previous linear golden-path parad...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Overlap of public genomic tracks with genome assembly gaps of hg19 and hg38. Overlap of public genom...
<p>Details of discordant variants from whole genome and exome sequencing data.</p
Additional file 3. Chromosome-level assemblies from diverse clades reveal limited structural and gen...
<p>Gaps in the genome of isolate 70-15 filled with sequences from the field isolates P131 and/or Y34...
This repository contains code used in data processing, quality control, analysis and visualisation p...
This repository contains code used in - Data quality check and pre-GWAS prep Genome-wide associa...
This is an archived version of a code repository (https://bitbucket.org/4dnucleome/spatial_chromatin...
The uploaded file contains Supplementary Tables S1-S61 for the manuscript "Assembly of 43 human Y ch...
Supplemental data and code related to the manuscript: "Multifactorial heterogeneity of the huma...
Supplemental Material for Prevalence of chromosomal abnormalities identified by copy number variatio...
Statistics of variant analysis in heterozygous sites in genome of CBS 11270 and between genomes of C...
<p>Exome sequence variants shared by all affected individuals in homozygous or compound heterozygous...
<p>The gene distribution of the 446 identified variants in the mtDNA genomes.</p
BACKGROUND: The last two human genome assemblies have extended the previous linear golden-path parad...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
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