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Clark_BioMorgan
Clark_BioMorgan
Reputation:
50 (New)
Joined:
11.4 years ago
Last seen:
2.3 years ago
Location:
Turkey
Latest posts by user
0 votes
2 replies
972 views
dbNSFP4.7a database format to Annovar Format?
snp annovar ngs dbnsfp
updated by Ram 4.5K • | written by Clark_BioMorgan 5
1 vote
1 reply
1.4K views
WisecondorX (NIPT) np.array( ValueError)?
numpy ngs wisecondorx nipt
updated by GenoMax 16K • | written by Clark_BioMorgan 5
0 votes
1 reply
6.0K views
bcl2fastq error? (bcl2fastq::common::InputDataError)
bcl2fastq nextseq illumina fastq
updated by Ram 4.5K • | written by Clark_BioMorgan 5
0 votes
2 replies
1.4K views
How to get a report like stuff of a bam file how many percent of the exons are coverred?
bam exon ngs miseq
updated by WouterDeCoster 4.8K • | written by Clark_BioMorgan 5
0 votes
0 replies
1 view
Comment: C: How to Get only one annotation with the SnpEff annotation?
written by Clark_BioMorgan 5
0 votes
3 replies
3.2K views
How to Get only one annotation with the SnpEff annotation?
snp annotation snpeff variation
updated by Pierre Lindenbaum 17K • | written by Clark_BioMorgan 5
0 votes
1 reply
2.1K views
How to get all variants in original BAM file with HaplotypeCaller? (No correction and BAMout)
variant calling haplotypecaller sequencing bamout
written by Clark_BioMorgan 5
0 votes
4 replies
1 view
Comment: C: Is there a way to save a specific Gene in IGV of a whole exome sample?
written by Clark_BioMorgan 5
0 votes
9 replies
2.6K views
Is there a way to save a specific Gene in IGV of a whole exome sample?
bam igv sequence
updated by sacha 250 • | written by Clark_BioMorgan 5
0 votes
0 replies
0 views
Comment: C: No mutations in BAM (IGV) but a mutation in final VCF?
written by Clark_BioMorgan 5
1 vote
1 reply
0 views
Comment: C: No mutations in BAM (IGV) but a mutation in final VCF?
written by Clark_BioMorgan 5
0 votes
2 replies
0 views
Comment: C: No mutations in BAM (IGV) but a mutation in final VCF?
written by Clark_BioMorgan 5
0 votes
9 replies
3.6K views
No mutations in BAM (IGV) but a mutation in final VCF?
bam igv variant calling gatk haplotypecaller
updated by WouterDeCoster 4.8K • | written by Clark_BioMorgan 5
0 votes
2 replies
3.2K views
Annovar annotation with refGene Database How to Dismiss Exon number and Gene Symbol from AAchange Column?
annovar refgene database variant calling aachange
updated by Biostar 380 • | written by Clark_BioMorgan 5
0 votes
1 reply
0 views
Comment: C: Only the longest transcript while annotating with Annovar?
written by Clark_BioMorgan 5
1 vote
3 replies
3.1K views
Only the longest transcript while annotating with Annovar?
annovar annotation snp transcript refgene
updated by Kevin Blighe 9.0K • | written by Clark_BioMorgan 5
0 votes
1 reply
1.9K views
What is the most usefull and up to date Prokaryotic Genome annotation Pipeline?
genome annotation ngs prokaryote wgs
updated by Philipp Bayer 888 • | written by Clark_BioMorgan 5
0 votes
1 reply
1.9K views
Is it possible to manipulate Chromatogram ?
chromatogram sanger abi fastq
updated by Ram 4.5K • | written by Clark_BioMorgan 5
0 votes
1 reply
0 views
Comment: C: Viral Whole genome Deep Sequencing within Human Host
written by Clark_BioMorgan 5
0 votes
3 replies
2.0K views
Viral Whole genome Deep Sequencing within Human Host
genome sequencing next-gen virus deep sequencing
written by Clark_BioMorgan 5
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