Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Profile
Posts
Awards
Show
all
questions
tools
blogs
news
tutorials
forum
answers
comments
Showing :
comments
0
votes
0
replies
84k
views
Comment:
C: Piping With Samtools, Bwa And Bedtools
updated 4.3 years ago by
Ram
43k • written 8.3 years ago by
alons
▴ 270
0
votes
0
replies
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
0
replies
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
1
reply
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
0
replies
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
0
replies
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
0
replies
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
alons
▴ 270
0
votes
0
replies
4.6k
views
Comment:
C: MAGERI: a software tool for calling rare variants and detecting circulating tumo
5.2 years ago by
alons
▴ 270
0
votes
1
reply
4.6k
views
Comment:
A: MAGERI: a software tool for calling rare variants and detecting circulating tumo
5.3 years ago by
alons
▴ 270
0
votes
1
reply
11k
views
Comment:
C: Help with understanding CNVkit output
updated 5.6 years ago by
Ram
43k • written 8.2 years ago by
alons
▴ 270
0
votes
1
reply
11k
views
Comment:
C: Help with understanding CNVkit output
updated 5.6 years ago by
Ram
43k • written 8.2 years ago by
alons
▴ 270
0
votes
0
replies
12k
views
Comment:
C: annotation of SV (structural variants)
6.2 years ago by
alons
▴ 270
0
votes
1
reply
12k
views
Comment:
C: annotation of SV (structural variants)
6.2 years ago by
alons
▴ 270
0
votes
0
replies
4.0k
views
Comment:
C: CNVKIT import errors
6.3 years ago by
alons
▴ 270
0
votes
0
replies
4.0k
views
Comment:
C: CNVKIT import errors
6.3 years ago by
alons
▴ 270
1
vote
1
reply
6.6k
views
Comment:
C: Annotation of Structural Variants and CNVs
8.0 years ago by
alons
▴ 270
0
votes
1
reply
6.6k
views
Comment:
C: Annotation of Structural Variants and CNVs
8.0 years ago by
alons
▴ 270
1
vote
0
replies
10k
views
Comment:
C: bwa mem seq and Segmentation fault (core dumped)
8.1 years ago by
alons
▴ 270
1
vote
0
replies
2.0k
views
Comment:
C: Variant annotation tool
8.1 years ago by
alons
▴ 270
0
votes
0
replies
3.5k
views
Comment:
C: Can I bulid a new reference for bwa ?
8.1 years ago by
alons
▴ 270
0
votes
1
reply
6.6k
views
Comment:
C: Annotation of Structural Variants and CNVs
8.1 years ago by
alons
▴ 270
0
votes
1
reply
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.1 years ago by
alons
▴ 270
0
votes
0
replies
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.2 years ago by
alons
▴ 270
0
votes
1
reply
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.2 years ago by
alons
▴ 270
0
votes
1
reply
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.2 years ago by
alons
▴ 270
0
votes
0
replies
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.2 years ago by
alons
▴ 270
0
votes
0
replies
7.1k
views
Comment:
C: Tools for SV & CNV detection
8.2 years ago by
alons
▴ 270
1
vote
0
replies
5.7k
views
Comment:
C: How can I add OMIM and HGMD data file on action right away to my VCF file?
8.4 years ago by
alons
▴ 270
0
votes
1
reply
5.0k
views
Comment:
C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
8.4 years ago by
alons
▴ 270
1
vote
0
replies
4.4k
views
Comment:
C: Lower GATK's HaplotypeCaller threshold for allele frequency as part of variant c
8.8 years ago by
alons
▴ 270
0
votes
1
reply
4.4k
views
Comment:
C: Lower GATK's HaplotypeCaller threshold for allele frequency as part of variant c
8.8 years ago by
alons
▴ 270
0
votes
0
replies
3.7k
views
Comment:
Comment: GATK recalibration, duplicates & realignment
updated 16 months ago by
Ram
43k • written 8.9 years ago by
alons
▴ 270
32 results • Page
1 of 1
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6