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Manuel
Manuel
Reputation:
50
Joined:
4.8 years ago
Last seen:
1.2 years ago
Location:
United Kingdom
Latest posts by user
0 votes
1 reply
781 views
Installing VEP for a Specific Chromosome (e.g., Chromosome 1) is not possible??
vep
updated by dthorbur dthorbur • written by Manuel • Manuel
0 votes
1 reply
927 views
Issue with picard index in my one chr reference fasta file
samtofastq
written by Manuel • Manuel
0 votes
0 replies
0 views
Comment: Comment: adding transcripts ID to the REVEL score
written by Manuel • Manuel
0 votes
1 reply
1.4K views
adding transcripts ID to the REVEL score
annotation revel
written by Manuel • Manuel
2 votes
0 replies
0 views
Answer: Answer: Why SpliceAI does not annotate variants in different transcripts as SpliceAI loo
written by Manuel • Manuel
0 votes
1 reply
1.5K views
Why SpliceAI does not annotate variants in different transcripts as SpliceAI lookup does.
spliceai
written by Manuel • Manuel
0 votes
2 replies
3.4K views
VEP with CONDA, installing annotation sources manually, what is the right directory to save the sources?
conda vep
updated by dariober dariober • written by Manuel • Manuel
0 votes
1 reply
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
0 votes
0 replies
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
0 votes
0 replies
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
0 votes
1 reply
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
0 votes
1 reply
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
0 votes
1 reply
0 views
Comment: Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
written by Manuel • Manuel
1 vote
15 replies
3.9K views
Interesting discrepancy between NGS (Illumina) and Sanger seq.
ngs sanger illumina variant
updated by barslmn • barslmn • written by Manuel • Manuel
0 votes
0 replies
750 views
ANNOVAR annotates delition and duplications with different co-ordinates
snpeff vep annovar
written by Manuel • Manuel
0 votes
1 reply
936 views
The number of unique SNPs and indels in Clinvar
clinvar
updated by GenoMax GenoMax • written by Manuel • Manuel
0 votes
0 replies
0 views
Comment: Comment: A efficient way to simulate bedtools interset with python
written by Manuel • Manuel
0 votes
0 replies
0 views
Comment: Comment: How to get the genomic coordinates of a transcripts in EntrezDirect ?
written by Manuel • Manuel
0 votes
1 reply
0 views
Comment: Comment: How to get the genomic coordinates of a transcripts in EntrezDirect ?
written by Manuel • Manuel
0 votes
5 replies
1.6K views
How to get the genomic coordinates of a transcripts in EntrezDirect ?
entrezdirect
written by Manuel • Manuel
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