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LAST/Poretools - where to start?
alignment next-gen sequencing written 3.3 years ago by omer.k40 • updated 1 day ago by Biostar ♦♦ 20
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ChIP-seq reads for the human genome
genome alignment chip-seq human sequencing written 2 days ago by sindhujamohan920 • updated 2 days ago by genomax80k
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16S reads comparing
next-gen rna-seq sequencing written 2.1 years ago by luyang100520 • updated 3 days ago by Biostar ♦♦ 20
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how to split forward and reverse reads from sam file
assembly alignment sequencing written 5 days ago by mejait9920 • updated 5 days ago by genomax80k
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fastqc duplicate reads
sequencing written 5 days ago by evelyn90 • updated 5 days ago by WouterDeCoster43k
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RNA read alignment using transcriptome
sequencing written 5 days ago by evelyn90 • updated 5 days ago by ATpoint31k
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Fastqc shows error message
genome assembly next-gen sequencing written 5 days ago by mejait9920 • updated 5 days ago by ATpoint31k
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Per Base Sequence Content
genome sequencing sequence fastqc written 7 days ago by Negin0 • updated 7 days ago by wm280
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Extract deletion positions from a SAM file
genome sequencing written 9 days ago by egill.richard0 • updated 9 days ago by Pierre Lindenbaum127k
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How to analyze DNA data with UMI
bioinformatics umi next-gen sequencing written 9 days ago by deniselavezzari0 • updated 9 days ago by genomax80k
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Split a large VCF into user defined regions
vcf vcftools sequencing written 3.5 years ago by zelia.worman0 • updated 10 days ago by nmzt430
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Human DNA - Sequenced by Multiple Labs
sequencing written 10 days ago by abnerapsley0 • updated 10 days ago by genomax80k
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