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1 vote
2 answers
627 views

Time for running ADMIXTURE analysis

1 vote
1 answer
42 views

Are there any simple ways to call copy number variants from a Nebula Genomics WGS data?

1 vote
0 answers
4 views

Passing data from the Agilent Trimmer utility to bwa-mem2 via a named pipe

0 votes
1 answer
15 views

PCA of bulk RNA-seq doesn't show clustering and show large variation in general

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0 answers
6 views

Are the odds of mutating the same single nucleotide in subsequent breedings multiplicative, or stand alone?

1 vote
1 answer
707 views

Changing transparency of markers in Chimera X

2 votes
1 answer
23 views

Overlay pathway over a set of genes in Cytoscape

4 votes
1 answer
64 views

Replicating VCF Filtering & Trait-Based SNP Extraction Workflow

0 votes
1 answer
30 views

how to see pacbio reads in IGV

3 votes
2 answers
1k views

How does DeepVariant construct RGB images from DNA sequences?

3 votes
4 answers
2k views

Retrieving NCBI Taxa IDs from refseq or GenBank assembly accession

1 vote
1 answer
17 views

Where to obtain fastq_illumina_filter

2 votes
1 answer
21 views

GBS- 'Failure' in, Per base sequence content, Sequence Duplication Levels, and Adapter Content

1 vote
1 answer
37 views

Indexing the reference genome my process is killed

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