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How to know if a variant is sequencing or mapping artifact?
variant vcf file freebayes written 24 minutes ago by kspata10 • updated 6 minutes ago by finswimmer2.8k
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Genome assembly and annotation
assembly written 49 minutes ago by biodano.geo0 • updated 11 minutes ago by Philipp Bayer5.5k
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taxid to genome refseq accession number
genome taxid refseq accession number genome written 2 hours ago by ruchikabhat3130 • updated 1 hour ago by genomax50k
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1
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40
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1
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Mapping paired-end reads to a draft genome using HISAT2
genome guided alignment rna-seq hisat2 written 3 hours ago by Farbod3.1k • updated 3 hours ago by genomax50k
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93
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70
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De novo assembly programm
assembly written 12 hours ago by Toto2610
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48
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p-values in GTEx
gene expression snp written 13 hours ago by kakukeshi20
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65
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1
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Can't find chr1 in a large fasta file using samtools/htsjdk
fasta assembly reference samtools written 13 hours ago by ljw10010 • updated 11 minutes ago by Eric Lim600
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BGIseq 500 - raw data files
bcl bgi written 16 hours ago by Gennady Khvorykh80
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46
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1
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image j measurement
software error written 19 hours ago by panteamohammadi180 • updated 18 hours ago by Alex Reynolds24k
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How to calculate read frequency from raw count data
R rna-seq written 22 hours ago by vkgaur2520 • updated 15 hours ago by Devon Ryan81k
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"methods.rdb' is corrupt" for every library I load
software error R written 1 day ago by demoraesdiogo20170 • updated 1 day ago by Kevin Blighe21k
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145
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Plotting the expression values for two genes in a range of cells
R ggplot2 written 1 day ago by Za40 • updated 15 hours ago by egeulgen280
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70
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Trimming reads of Chipseq samples
alignment chip-seq written 1 day ago by GK161030 • updated 15 hours ago by Devon Ryan81k
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128
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99
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5 follow
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Is there a perfect WGS dataset?
next-gen sequence written 1 day ago by marongiu.luigi190 • updated 1 day ago by Pierre Lindenbaum108k
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167
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107
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Processing ATAC-seq data after peak calling
peak calling sequencing written 1 day ago by anais139610 • updated 1 day ago by James Ashmore2.4k
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141
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107
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