Showing: dna-seqreset
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Is there any reason not to run RS_ReadsOfInsert?
genome ccs rsii dna-seq pacbio written 20 days ago by conrad.stack0 • updated 19 days ago by Charles Warden4.8k
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creating rarefaction curves
R metagenomics dna-seq written 2.9 years ago by Phil S.610 • updated 8 weeks ago by Biostar ♦♦ 20
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ExAC PLI score calculation
dna-seq written 12 weeks ago by jonessara7700
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known unmappable or poorly sequenced regions in hg38
bed ngs dna-seq written 3 months ago by Paul530 • updated 3 months ago by igor4.1k
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News: NCBI NOW (Next generation sequencing Online Workshop) October 13 - 23 , 2015
ncbi news mapping ngs rna-seq dna-seq written 20 months ago by rtliu1.9k • updated 6 months ago by DCGenomics280
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How to annotate CNV events with gene information?
cnv events annovar dna-seq rna snp written 6 months ago by bioinforesearchquestions80 • updated 6 months ago by Amitm1.3k
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Difference between primary nad capture targets
targets dna-seq capture written 6 months ago by John50 • updated 6 months ago by WouterDeCoster17k
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News: How to analyze NGS data: An overview of nine different IT solutions
ngs dna-seq news rna-seq written 6 months ago by David Langenberger7.8k • updated 6 months ago by Lars430
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Software SVS for DNA-seq
dna-seq cattle svs rna-seq written 7 months ago by gabriela.ribeiro.br0 • updated 7 months ago by genomax27k
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Biopython construct a sequence from multiple reads
dna-seq biopython multiple reads written 10 months ago by sefu20 • updated 10 months ago by Daniel3.3k
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Is Paired End analysis possible with FASTQC?
paired-end dna-seq qc fastqc written 12 months ago by chefarov50 • updated 10 months ago by Biostar ♦♦ 20
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