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How to know if a variant is sequencing or mapping artifact?
variant vcf file freebayes written 2 hours ago by kspata10 • updated 1 hour ago by finswimmer2.8k
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Can't find chr1 in a large fasta file using samtools/htsjdk
fasta assembly reference samtools written 16 hours ago by ljw10010 • updated 2 hours ago by Eric Lim600
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Genome assembly and annotation
assembly written 2 hours ago by biodano.geo0 • updated 2 hours ago by Philipp Bayer5.5k
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taxid to genome refseq accession number
genome taxid refseq accession number genome written 4 hours ago by ruchikabhat3130 • updated 3 hours ago by genomax50k
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Mapping paired-end reads to a draft genome using HISAT2
genome guided alignment rna-seq hisat2 written 5 hours ago by Farbod3.1k • updated 5 hours ago by genomax50k
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Has Anyone Tried Rum For Aligning/Counting Illumina Rna-Seq Data?
alignment rna written 6.9 years ago by Travis2.8k • updated 5 hours ago by Biostar ♦♦ 20
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 18 months ago by Istvan Albert ♦♦ 77k • updated 5 hours ago by Vijay Lakhujani2.5k
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De novo assembly programm
assembly written 14 hours ago by Toto2610
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p-values in GTEx
gene expression snp written 15 hours ago by kakukeshi20
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Trimming reads of Chipseq samples
alignment chip-seq written 1 day ago by GK161030 • updated 17 hours ago by Devon Ryan81k
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How to calculate read frequency from raw count data
R rna-seq written 1 day ago by vkgaur2520 • updated 17 hours ago by Devon Ryan81k
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