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<prev • 4,297 results • page 1 of 144 • next >
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Losing somatic SNPs
varscan snp varaft written 28 days ago by gab • 0 • updated 3 hours ago by Biostar ♦♦ 20
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1
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81
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1
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SNPs genomic classification based on VCF annotation
R snp written 7 hours ago by aarvaBioinfo • 10 • updated 4 hours ago by finswimmer ♦ 4.5k
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maftools - no chromosomal coordinates
R bioconductor snp written 16 hours ago by sumithrasank75 • 90 • updated 13 hours ago by zx8754 ♦ 4.8k
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how to detect mutation from viral RNA-seq data
R rna-seq snp sequencing written 15 hours ago by babasaraki • 0 • updated 14 hours ago by grant.hovhannisyan • 1.0k
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6 follow
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Tool: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing runs in Sequence Read Archive
chip-seq snp rna-seq tool written 7 days ago by btsui • 230
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1
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92
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Extract SNPs from VCFfile located in genes based on GFF file information
gene snp written 18 hours ago by Denis • 30 • updated 17 hours ago by finswimmer ♦ 4.5k
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3
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Kissplice: Problem getting SNPs in test data
snp kissplice written 4 months ago by WeepingMeadow • 0 • updated 19 hours ago by leandro.ishi.lima • 80
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1
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60
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1
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Subset analyze of multiple sample file in PLINK 1.9
sequence plink snp written 1 day ago by mike229lin • 10 • updated 20 hours ago by zx8754 ♦ 4.8k
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Variant training set for Zebrafish to apply GATK VariantRecalibrator
gatk ngs zebrafish genotyping-by-sequencing snp written 1 day ago by Matthias • 20
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1
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108
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1
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Best technique for CNV and mutation analysis
snp sequencing written 1 day ago by neuro3030 • 0
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Nan in expectationUNR
software error gene snp genome written 23 months ago by yxwang6 • 0 • updated 1 day ago by emamy202 • 0
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3
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7 follow
3
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how can i remove duplicated variants from vcf file?
vcf snp written 13 months ago by kk.mahsa • 70 • updated 3 days ago by Shicheng Guo • 6.1k
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Characterization of the insecticide resitance mechanism
snp written 3 days ago by mahnazkiani • 40
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Extract a list of SNPs from a BCF file
bcf snp written 3 days ago by Fersal • 0 • updated 3 days ago by genomax ♦ 54k
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Use PacBio's iso-seq data to look for variant
next-gen snp sequencing written 2.2 years ago by yanweng • 30 • updated 4 days ago by Biostar ♦♦ 20
2
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1
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Bcftools view options for SNPs calling.
bcftools samtools snp mpileup written 3.1 years ago by Eddie_I • 10 • updated 4 days ago by Kevin Blighe ♦ 26k
2
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1
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132
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1
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Variant Allele Frequency
vcf samtools snp written 5 days ago by kspata • 30 • updated 4 days ago by btsui • 230
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what value reflect the admixture dates in the logfile Using ALDER
alder admixture time snp written 10 weeks ago by zhangmingpeng • 0 • updated 4 days ago by Biostar ♦♦ 20
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1
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130
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1
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How calculate MAF from impute2 output in R
maf impute2 snp written 7 weeks ago by vgenepi • 10 • updated 4 days ago by zx8754 ♦ 4.8k
1
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1
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98
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1
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How to investigate reference and alternative alleles of many SNPs
snp written 5 days ago by Apprentice • 10
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1
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118
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5 follow
1
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convert Rate(cM/Mb) to probability
rate(cm/mb) recombination probability hotspots snp written 6 days ago by katkota.a • 0
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Eagle error: Haploid genotype found
gwas next-gen imputation snp written 6 days ago by myses030566 • 0
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1
answer
82
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1
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What's the difference between the /rest/variant and /rest/variant/variant requests to the Exac API?
api variant exac snp written 6 days ago by kynnjo • 20 • updated 6 days ago by finswimmer ♦ 4.5k
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107
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Short Variants calling error when using bcftools mpileup
genome alignment snp written 6 days ago by mike229lin • 10 • updated 6 days ago by finswimmer ♦ 4.5k
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77
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PRSice: Imputation and clumping
prsice gwas polygenic risk score snp written 6 days ago by muraved • 0
3
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1
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105
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1
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How to predict the effect of DNA base deletion on protein?
gene snp written 7 days ago by abc.faisal • 0
6
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1
answer
129
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1
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What is the difference between HaplotypeCaller and UnifiedGenotyper?
snp written 7 days ago by mostafarafiepour • 0 • updated 7 days ago by finswimmer ♦ 4.5k
1
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1
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106
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1
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Updating INDEL SNP positions
snp written 7 days ago by drakejh • 0 • updated 7 days ago by finswimmer ♦ 4.5k
6
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2
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RNA-seq experimental design for SNP calling
rna-seq snp written 12 months ago by windhavenn • 20 • updated 8 days ago by andrew.j.skelton73 ♦ 5.2k
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SNP Files to VCF files in terminal window
vcf genome snp terminal rna-seq written 8 days ago by Sa • 0
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