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<prev • 4,584 results • page 1 of 153 • next >
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how to transfer SNV file to plink format
snp written 2 days ago by LZhang • 0 • updated 10 hours ago by zx8754 ♦ 6.0k
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Haplotype block in PLINK using r2 values
haplotypes snp plink ld written 10 hours ago by GabrielMontenegro • 430
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How to produce fasta sequence from haplotyping (illumina)
snp written 1 day ago by luc.cornet • 0 • updated 1 day ago by WouterDeCoster ♦ 35k
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1
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I16 Info Tag
bcftools snp mpileup sequencing written 2 days ago by tbb21 • 0 • updated 1 day ago by finswimmer ♦ 7.8k
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What is a bad GATK Genotype Quality?
quality snp written 3.5 years ago by devenvyas • 520 • updated 1 day ago by Biostar ♦♦ 20
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Evaluate nucleotide and haplotype diversity using sequences from single-pool RAD data
interspecies comparisons snp nucleotide diversity written 8 months ago by chrys.delord • 0 • updated 3 days ago by Biostar ♦♦ 20
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Are my methods correct?
genome rna-seq snp written 3 days ago by ishmahe16 • 0 • updated 3 days ago by WouterDeCoster ♦ 35k
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Convert matrix in numeric format to genotype format
snp written 3 days ago by shinken123 • 80 • updated 3 days ago by chrchang523 ♦ 4.3k
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Some question about mutmap, please help
genome alignment snp written 3 days ago by Zeason • 0
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5 follow
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Merge vcf files with multiple samples into one vcf with all variants
snp written 3 days ago by bioinfo89 • 40 • updated 3 days ago by WouterDeCoster ♦ 35k
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How to incorporate interaction between two alleles in ApoE for Alzheimer's polygenic risk score?
snp written 3 days ago by rkl • 0
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1
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1
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Ensembl variation ancestral allele data
ancestral snp ensembl written 4 days ago by Scott • 70 • updated 3 days ago by Emily_Ensembl ♦ 16k
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VCFtools calculate SNP density
vcf bioinformatics snp density vcftools snp written 3 days ago by christinachavez • 0 • updated 3 days ago by finswimmer ♦ 7.8k
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How do you find the number of SNPs per gene given a genotype and a map file?
gene R snp written 3 days ago by eternalshadowrose • 0
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1
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Databases and Variant Tools for Cancer Genes
gene database sequence snp variants written 4 days ago by ojelizodun • 0
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1
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MAQ install error
software error next-gen snp rna-seq written 4 days ago by Ashley • 10 • updated 4 days ago by h.mon ♦ 21k
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1
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120
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1
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Looking for human reference genome with ancestral SNP alleles
genome assembly hg38 snp ensembl written 5 days ago by Scott • 70 • updated 5 days ago by Emily_Ensembl ♦ 16k
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1
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1
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parsing Affymetrix file
assembly sequence snp written 5 days ago by john.anderson.ivy • 10
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1
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1
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Making nice plots based on the different metrics from VCF file
genome R snp written 5 days ago by Denis • 30 • updated 5 days ago by Pierre Lindenbaum ♦ 115k
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1
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1
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Where should I go to download human SNP reference data ? hg18_unmasked.plusContam.fa
genome next-gen snp ucsc written 5 days ago by Ashley • 10 • updated 5 days ago by ATpoint ♦ 10k
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Problem installing fcgene using cygwin64.
software error snp written 6 days ago by paulwjeffries • 0
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poly ploid consensus seq generation
genome assembly rna-seq snp written 6 days ago by fatimarasool135 • 0
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1
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Get Flanking Amino Acid Sequence
R dna-seq sequence snp python written 7 days ago by windsur • 10
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1
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CNV, CNA and SNP calling
cna cnv snp written 6 days ago by Pin.Bioinf • 170 • updated 6 days ago by Nicolas Rosewick ♦ 7.0k
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What's the difference between GWAS Catalog and COSMIC database ?
gwas snp written 10 days ago by hsiaoyi0504 • 40 • updated 6 days ago by Kevin Blighe ♦ 33k
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Extract vcf file header and save it in Key-Value csv
genome next-gen snp sequencing written 7 days ago by tinyskinn • 0
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Can I use VarScan for tumor_time2/tumor_time1 CNA and SNP calling?
cna varscan cnv snp written 6 days ago by Pin.Bioinf • 170
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Liftover errors with CrossMap and Picard
software error rna-seq snp written 6 days ago by rshoobs • 0
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1
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1
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Getting same SNPs both in cancer and normal files when seen in IGV
snp written 7 days ago by db351223 • 0 • updated 6 days ago by WouterDeCoster ♦ 35k
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How to count variant frequencies in set of vcf lists
vcf ngs snp sequencing written 7 days ago by sanna.gudmundsson • 0
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