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Answer: I'm not sure my Bulk RNAseq read counts extracted from fastq file are correct
2.5 years ago by
husensofteng
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Answer: Naïve question about LC-MS/MS proteomic datasets : looking for ressources, studi
2.6 years ago by
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Answer: how to merge two files in two columns using bash command lines
2.9 years ago by
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A: Create a database of RefSeq genes
3.7 years ago by
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C: genomic features 3'utr and 5'utr
3.9 years ago by
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C: Detecting potentially unannotated genes from RNA-seq alignments?
4.0 years ago by
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A: per sample mean coverage and standard deviation
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A: convert genome file to transcriptome file
4.9 years ago by
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A: Keeping only common variants in the merged VCF file
5.0 years ago by
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A: get GTEx mean expression by tissue
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A: Mapping SNP position to gff file
updated 5.0 years ago by
ATpoint
82k • written 5.0 years ago by
husensofteng
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A: Stringtie merge assembly with extra transcripts
5.0 years ago by
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A: How to access specifically 30x NA12878 sequencing runs
5.2 years ago by
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A: Example datasets for RNA-Seq Differential Expression Analysis
5.2 years ago by
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A: Trascription factor binding site prediction
5.2 years ago by
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