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Floris Brenk • 890
Status: New
Handle: @Floris Brenk9611
Reputation: 890
Email: f***********@hotmail.com
Joined: 8 months ago
Last seen: 9 months ago
Location: USA

about me

Rare variant meta-analyzing tests
0 Votes | 1 Reply
2.0 years ago
Floris Brenk
• 890
• updated 9 months ago
swetansu
• 0
Comment: C: Allele Frequency correlation in R
0 Votes | 0 Replies
4.0 years ago
Floris Brenk
• 890
• updated 17 months ago
RamRS
21k
Comment: C: Remove rows based on duplicates in one column
1 Vote | 1 Reply
4.0 years ago
Floris Brenk
• 890
• updated 17 months ago
RamRS
21k
Comment: C: XHMM GATK exome sequencing deletions genome wide or selected genes ?
0 Votes | 0 Replies
4.0 years ago
Floris Brenk
• 890
• updated 17 months ago
RamRS
21k
Add gene annotation/information to CNV plot in R
0 Votes | 1 Reply
2.3 years ago
Floris Brenk
• 890
• updated 2.3 years ago
cmdcolin
♦ 1.2k
Comment: C: ATACseq and HiC sequencing
0 Votes | 0 Replies
2.4 years ago
Floris Brenk
• 890
ATACseq and HiC sequencing
4 Votes | 7 Replies
2.4 years ago
Floris Brenk
• 890
• updated 2.4 years ago
Devon Ryan
90k
Comment: C: ATACseq and HiC sequencing
0 Votes | 1 Reply
2.4 years ago
Floris Brenk
• 890
Comment: C: How to make a nice mutation overview figure like this?
0 Votes | 0 Replies
2.5 years ago
Floris Brenk
• 890
Comment: C: How to make a nice mutation overview figure like this?
0 Votes | 0 Replies
2.5 years ago
Floris Brenk
• 890
Answer: A: Duplicate ID in bed file
0 Votes | 1 Reply
2.5 years ago
Floris Brenk
• 890
Output the call rate of genotypes in plink
2 Votes | 1 Reply
2.6 years ago
Floris Brenk
• 890
• updated 2.6 years ago
chrchang523
5.2k
Making a vcf file from a subset of regions from gvcf files
1 Vote | 1 Reply
2.6 years ago
Floris Brenk
• 890
• updated 2.6 years ago
aays
• 140
Comment: C: converting rows into columns and vice versa
0 Votes | 1 Reply
2.7 years ago
Floris Brenk
• 890
Comment: C: converting rows into columns and vice versa
0 Votes | 1 Reply
2.7 years ago
Floris Brenk
• 890
Comment: C: Chromosome Y imputation, any good reference panels?
0 Votes | 1 Reply
2.8 years ago
Floris Brenk
• 890
Comment: C: Cannot remove subjects from Plink files
0 Votes | 1 Reply
2.9 years ago
Floris Brenk
• 890
Answer: C: finding unique mutations from a multi-sample VCF
2 Votes | 0 Replies
2.9 years ago
Floris Brenk
• 890
Comment: C: How to annotate TTS or TES
0 Votes | 1 Reply
3.0 years ago
Floris Brenk
• 890
Comment: C: RNA seq library preparation, PCR cycles
0 Votes | 0 Replies
3.0 years ago
Floris Brenk
• 890
Detect chromosome abnormalities in WGS
1 Vote | 8 Replies
3.3 years ago
Floris Brenk
• 890
• updated 3.2 years ago
Biostar
20
Comment: C: vcftools merge files problem
0 Votes | 1 Reply
3.2 years ago
Floris Brenk
• 890
Comment: C: vcftools merge files problem
0 Votes | 1 Reply
3.2 years ago
Floris Brenk
• 890
Comment: C: risk value with genetic data
0 Votes | 0 Replies
3.2 years ago
Floris Brenk
• 890
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