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HT-seq - what is ideal?
rna-seq written 1 hour ago by junsionglow20
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SNPs genomic classification based on VCF annotation
R snp written 3 hours ago by aarvaBioinfo10 • updated 44 minutes ago by finswimmer4.5k
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(Closed) samtools error #E27
samtools written 4 hours ago by michael0
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Choosing a ChIP-seq control for Encode pipeline?
encode chip-seq written 5 hours ago by gewa0 • updated 4 hours ago by Alex Reynolds25k
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samtools error #E27
samtools written 6 hours ago by michael0 • updated 6 hours ago by Ram17k
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63
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Grail: reflow on AWS vs others (snakemake/cfncluster, etc)
aws workflow snakemake reflow cfncluster written 8 hours ago by isaacyho0 • updated 7 hours ago by btsui230
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how to detect mutation from viral RNA-seq data
R rna-seq snp sequencing written 11 hours ago by babasaraki0 • updated 10 hours ago by grant.hovhannisyan1.0k
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maftools - no chromosomal coordinates
R bioconductor snp written 12 hours ago by sumithrasank7590 • updated 9 hours ago by zx87544.8k
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132
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Could someone explain this perl command?
perl bash written 12 hours ago by Seq22550
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Extract SNPs from VCFfile located in genes based on GFF file information
gene snp written 14 hours ago by Denis30 • updated 13 hours ago by finswimmer4.5k
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Merge vcf files of structural variants
vcf merge structural_variants written 15 hours ago by ma170 • updated 14 hours ago by WouterDeCoster31k
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199
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5 follow
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How to convert fasta file format to phylip file format
fasta R phylogenetic tree phylip ggtree written 16 hours ago by Mike1.0k • updated 9 hours ago by zx87544.8k
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5 follow
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Boxplot each row in a dataset in R?
boxplot dataset plot R cancer written 18 hours ago by bio9440 • updated 16 hours ago by cpad01128.3k
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Salmon Algorithm Binary Search
salmon written 19 hours ago by vincentpailler30 • updated 10 hours ago by Rob2.5k
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2
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Subset analyze of multiple sample file in PLINK 1.9
sequence plink snp written 21 hours ago by mike229lin10 • updated 16 hours ago by zx87544.8k
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261
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