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blast -seqidlist is slow
blast written 25 minutes ago by gb50
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fastq- dump error
software error sequence rna-seq written 1 hour ago by k.kathirvel9350 • updated 55 minutes ago by finswimmer2.9k
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WGCNA network with condition and normal samples
wgcna network rna-seq written 2 hours ago by saptarathideb0 • updated 1 hour ago by Jacob Warner600
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36
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TCGA raw data (Level 1)
copy number rna-seq snp written 3 hours ago by H.Hasani590
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51
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TCGA purity data
tcga ascat purity written 3 hours ago by Folder40g110
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NCBI Genome Remapping Service- clinical remap
co-ordinate remapping snp written 4 hours ago by Sudhir Jadhao50 • updated 4 hours ago by Vijay Lakhujani2.6k
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STAR alignment command.
assembly sequence rna-seq alignment written 6 hours ago by amitunited05320 • updated 4 hours ago by b.nota4.0k
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Lists of ncRNAS for cow, yeast
ncrna written 7 hours ago by blur90 • updated 2 hours ago by genomax50k
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htslib installation problem
augustus busco htslib written 7 hours ago by kabir.deb03530 • updated 4 hours ago by ag1805x80
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Creating your own substitution matrix from an alignment
software error alignment written 7 hours ago by mdsiddra0 • updated 6 hours ago by Vijay Lakhujani2.6k
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Variant calling on RNA seq using GATK pipeline
rna-seq written 7 hours ago by renu18july0 • updated 6 hours ago by Vijay Lakhujani2.6k
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90
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Some questions about write human mitochondrial variants into VCF file
vcf mtdna written 8 hours ago by MatthewP0 • updated 3 hours ago by Pierre Lindenbaum108k
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How to know if a variant is sequencing or mapping artifact?
vcf variant freebayes written 10 hours ago by kspata30 • updated 4 hours ago by finswimmer2.9k
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Genome assembly and annotation
assembly written 10 hours ago by biodano.geo0 • updated 6 hours ago by lieven.sterck1.7k
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Extract codon information from VCF file
R snp written 12 hours ago by k.rajain12120 • updated 6 hours ago by Nandini570
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taxid to genome refseq accession number
genome taxid refseq accession number genome written 12 hours ago by ruchikabhat3130 • updated 4 hours ago by Sej Modha2.9k
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