Showing: snpreset
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Making nice plots based on the different metrics from VCF file
genome R snp written 10 months ago by Denis120 • updated 5 hours ago by pwwang0
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47
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35
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how to merge gvcf using bcftools
snp written 6 hours ago by evelyn30
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78
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1
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Purines and pyrimidines in frame shift mutations
sequence snp sequencing written 3 days ago by 333509845910 • updated 10 hours ago by Cupton60
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SNPEff database building error
snp written 2.6 years ago by ntyagi6540 • updated 13 hours ago by trinidadmartinc0
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71
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bedtools and SNPs for pyseer-GWAS analysis
genome gene snp written 21 hours ago by 333509845910 • updated 19 hours ago by ATpoint24k
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34
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Best tool for variant calling in polyploids
genome assembly snp written 4 days ago by giannkas10 • updated 22 hours ago by harish230
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8 follow
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how to count variants par sample per chromosome in a vcf file?
snp written 13 months ago by nagarsaggi0 • updated 1 day ago by chrchang5235.7k
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83
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PLINK BED format: how interpret 0, 1, 2
plink snp written 11 days ago by CaffeSospeso40 • updated 1 day ago by chrchang5235.7k
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67
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4
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Linux: move/copy same name files to one folder
sequence snp written 2 days ago by 333509845910 • updated 2 days ago by Pierre Lindenbaum123k
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68
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78
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127
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gvcf error bcftools
snp written 4 days ago by evelyn30
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128
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1
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non-SNP variants in a vcf merge file
snp written 10 days ago by evelyn30 • updated 4 days ago by Kevin Blighe50k
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40
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68
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Plink --score generates different output for same dataset
software error gene next-gen snp written 7 days ago by ian15brown0 • updated 6 days ago by zx87548.3k
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5 follow
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What is the -nct alternative in GATK 4.0.0.0?
snp written 17 months ago by mostafarafiepour60 • updated 7 days ago by raf.marcondes20
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5
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71
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Allele discrepancy between Database and Publication
ensembl dbsnp genotype snp written 7 days ago by snp_guy0 • updated 7 days ago by Emily_Ensembl19k
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75
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96
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Separate SNP common
snp written 8 days ago by kasiriyan.m.m0
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103
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