Bioinformatics Stack Exchange is a question and answer site for researchers, developers, students, teachers, and end users interested in bioinformatics. It only takes a minute to sign up.

Sign up to join this community
Anybody can ask a question
Anybody can answer
The best answers are voted up and rise to the top

Explore our questions

1 vote
1 answer
75 views

Error Registering Job Definition AWS

0 votes
1 answer
23 views

Analysing the Effect of a Drug on the Morphological Changes of a Cell Type

2 votes
1 answer
75 views

Manta "--exome: command not found"

0 votes
0 answers
15 views

Dealing With Manta Limitations

0 votes
0 answers
9 views

RNAseq alignment: best practices for aligning to multiple isoforms?

0 votes
1 answer
14 views

Can you infer orientation from vcf file data?

3 votes
1 answer
38 views

Passing strings for password, email authentication and download link

0 votes
0 answers
10 views

How to check average gene expression for each of 2 conditions within a cluster in scanpy?

3 votes
0 answers
29 views

What is the NCBI's definition of an "atypical genome"?

2 votes
1 answer
33 views

Improving conversion of abricate tsv file to gff3 file

1 vote
1 answer
30 views

Running cellranger on scRNASeq data with feature barcoding (10x + antibody capture)

0 votes
1 answer
47 views

Help with analyzing SNP data for three patient groups

2 votes
1 answer
449 views

How do I include silent mutations in an oncoplot using maftools?

2 votes
1 answer
20 views

Using ticks on the x axis or a scale bar when visualisizing a phylogram?

Browse more Questions