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1 vote
0 replies
1.2K views
Job: Postdoc in Reproductive genetics - bioinformatics
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What is a recommended maximum read depth threshold for DNA variant filtration, supported by scientific articles?
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1 vote
13 replies
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How are probabilities of insertions and deletions encoded in FASTQ?
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low alignment rate for RNA-Seq data
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Optimal Computer Configuration for Bioinformatics Analysis
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641 views
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4 replies
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4 replies
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0 votes
1 reply
542 views
All VS All contamination check for tumor samples
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written by mps 0
0 votes
2 replies
789 views
Determine binding sites in unstimulated TF ChIP-seq samples
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0 votes
1 reply
598 views
GO analysis custom reference?
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2 replies
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0 votes
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611 views
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0 votes
3 replies
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0 votes
12 replies
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Phylogenetic tree from whole genome using BUSCO
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0 votes
0 replies
600 views
News: Course on Ancient Metagenomics - online, 27-29 May
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0 votes
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0 replies
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From Cram to gVCF
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2 votes
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R CytoTRACE2 Results: Potency Score of Naive B Cells Lower Than Memory B and Plasmablasts – Contradicts Biological Knowledge
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2 votes
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Rules for Assigning Start and End Phase to Coding Exons
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0 votes
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converting transcript positions to genomic locations
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0 votes
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simulate a genome with specific event
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4 replies
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1 reply
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0 replies
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Help with Finding SNPs in H. pylori Assembled Genomes
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878 views
Keep SNP's with call rate greater than 30 in VCF
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Dynamic tree cut results
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0 votes
0 replies
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filtering heterozygous genotypes
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881 views
An alternative to haplotype phasing - assembly?
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0 votes
0 replies
592 views
how to make/get the SNP annotation file for running TORUS
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