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Finding SNPs per gene for SNP Density in UNIX
varscan grep unix snp written 3.5 years ago by crawlthrutacos0 • updated 31 minutes ago by Biostar ♦♦ 20
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DEG and low counts
rnaseq deseq2 ma plot low-counts written 2 hours ago by NielQC10
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error RepeatMasker Installation
perl written 4 hours ago by frida0 • updated 3 hours ago by genomax65k
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Count number of monophyletic groups within pylogeny
phylogeny monophyletic written 8 hours ago by Darill20 • updated 3 hours ago by jrj.healey11k
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R analysis for read counts using edgeR
rna-seq written 6 hours ago by Liftedkris0 • updated 4 hours ago by ATpoint15k
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 2.4 years ago by Istvan Albert ♦♦ 80k • updated 4 hours ago by Baby Bioinformatician20
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fastqc of chipseq dataset - two peaks in GC content
gc content peaks chip-seq fastqc written 29 days ago by Assa Yeroslaviz1.2k • updated 6 hours ago by Biostar ♦♦ 20
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how to remove pig sequences from metagenomics data
next-gen written 8 weeks ago by g.feng0 • updated 12 hours ago by Biostar ♦♦ 20
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Assembler for only nanopore data
assembly genomics abyss ont written 3 days ago by ringourquia10 • updated 14 hours ago by harish180
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XPEHH output file blank in SELSCAN
snp written 8 weeks ago by azizul0 • updated 18 hours ago by Biostar ♦♦ 20
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"high" quality RNA but poor RNAseq results
rna-seq written 21 hours ago by CrazyB210 • updated 19 hours ago by Charles Warden6.6k
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bcf convert 23andme to vcf
bcftools snp written 10 days ago by stuartkkim0
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Exacting all the headers in a fasta file using R
R sequence written 22 hours ago by xuenanwang0 • updated 20 hours ago by Pierre Lindenbaum119k
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Help a SNP newbie out
genome software error sequencing snp assembly written 20 hours ago by sarah.goldstein0 • updated 20 hours ago by Pierre Lindenbaum119k
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PLINK vcf to binary files error: Unused command line option: --vcf
vcf plink genomics written 21 hours ago by jon.klonowski0 • updated 20 hours ago by chrchang5234.9k
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