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
1.1k
views
Comment:
C: Merging genomic databases from different intervals (GenomicsDBImport)
3.3 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
2.0k
views
Comment:
C: Is there a database of haploinsufficiency scores or status for each gene?
3.6 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.8k
views
Comment:
C: Discrepancy between UCSC table browser PhyloP score and Bedmap mapped PhyloP sco
3.9 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.6k
views
Comment:
C: Figure out genotype from VCF line
updated 3.9 years ago by
Ram
43k • written 3.9 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.6k
views
Comment:
C: combining / merging overlapping reads in bam file to one in silico long read
4.0 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
1.5k
views
Comment:
C: What's the best way to serve VCF data on web?
4.1 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
3.6k
views
Comment:
C: Combining VCF files using GATK
4.1 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
1.2k
views
Comment:
C: Flanking sequence retreival
4.3 years ago by
rbagnall
★ 1.8k
1
vote
2
replies
3.4k
views
Comment:
C: gene identification by exome seq of case control
updated 4.3 years ago by
Ram
43k • written 10.0 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
2.7k
views
Comment:
C: How can I find the most studied SNP of a gene?
updated 4.3 years ago by
Ram
43k • written 8.3 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
3.1k
views
Comment:
C: LOD score of a single genotype
updated 4.4 years ago by
Ram
43k • written 8.4 years ago by
rbagnall
★ 1.8k
2
votes
1
reply
1.1k
views
Comment:
C: Is 1 deleted T in a T stretch always detected, assuming enough coverage of cours
4.4 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.1k
views
Comment:
C: Is 1 deleted T in a T stretch always detected, assuming enough coverage of cours
4.4 years ago by
rbagnall
★ 1.8k
2
votes
0
replies
2.2k
views
Comment:
C: Number of snps are very low
updated 4.4 years ago by
Ram
43k • written 8.5 years ago by
rbagnall
★ 1.8k
1
vote
1
reply
1.6k
views
Comment:
C: VCF file format
updated 4.4 years ago by
Ram
43k • written 8.5 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
2.3k
views
Comment:
C: How many base pairs are there in All exon V4+UTR from Agilent manufacture?
updated 4.4 years ago by
Ram
43k • written 8.6 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.0k
views
Comment:
C: Large tab-delimited table of SNP data, how to filter out some rows based on rsID
updated 4.5 years ago by
Ram
43k • written 8.9 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
1.8k
views
Comment:
C: Extract variants from genomic range from gnomAD GRCh38
4.5 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
6.6k
views
Comment:
C: How can I download snp genotype file from 1000 Genome?
updated 4.5 years ago by
Ram
43k • written 9.2 years ago by
rbagnall
★ 1.8k
2
votes
0
replies
1.6k
views
Comment:
C: how can a DELETION be not a NULL variant?
4.8 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
9.7k
views
Comment:
C: Download all eQTL data for all the 9 tissues from GTEx Portal
4.9 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.1k
views
Comment:
C: How do we call this phenomenon in evolution?
5.4 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.7k
views
Comment:
C: no successful variants lifted over from hs37d5_plusRibo_plusOncoViruses_plusERCC
5.8 years ago by
rbagnall
★ 1.8k
1
vote
1
reply
2.9k
views
Comment:
C: Find Intersections Between ClinVar Track and VCF In IGV
5.8 years ago by
rbagnall
★ 1.8k
1
vote
1
reply
2.9k
views
Comment:
C: Find Intersections Between ClinVar Track and VCF In IGV
5.8 years ago by
rbagnall
★ 1.8k
3
votes
0
replies
2.3k
views
Comment:
C: Update RefSeq database with Ensembl VEP
5.9 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
1.3k
views
Comment:
C: How can I deal with this publication issue?
6.0 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
5.1k
views
Comment:
C: snpEff inappropriate interpretation of variants?
6.7 years ago by
rbagnall
★ 1.8k
6
votes
2
replies
54k
views
Comment:
C: How to extract specific chromosome from vcf file
7.8 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
1.5k
views
Comment:
C: Number of SNPs captured by targeted sequencing panels
8.0 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.5k
views
Comment:
C: Using VCFTools (v0.1.13) with ExAC (release 0.3.1)
8.1 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
6.6k
views
Comment:
C: From gene symbol list to their coordinates
8.1 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.6k
views
Comment:
Comment: eigensoft smartpca error "OOPS -i flag not specified at smartpca.perl line 21
updated 21 months ago by
Ram
43k • written 8.2 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
2.8k
views
Comment:
C: How to decide how broken a gene is
8.4 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
3.3k
views
Comment:
Comment: Whole exome length of exons from bam file
updated 19 months ago by
Ram
43k • written 8.6 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
4.9k
views
Comment:
Comment: Variant calling for MNP
updated 19 months ago by
Ram
43k • written 8.7 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
4.9k
views
Comment:
C: Variant calling for MNP
8.7 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.9k
views
Comment:
Comment: Variant calling for MNP
updated 19 months ago by
Ram
43k • written 8.7 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
5.9k
views
Comment:
Comment: vcf SNP file minor allele frequency filter?
updated 18 months ago by
Ram
43k • written 8.7 years ago by
rbagnall
★ 1.8k
1
vote
0
replies
18k
views
Comment:
Comment: Extract a particular data from text file using perl
updated 17 months ago by
Ram
43k • written 8.8 years ago by
rbagnall
★ 1.8k
0
votes
2
replies
4.1k
views
Comment:
C: What's the best way to find all the possible cutting sites of an sequence-specif
8.8 years ago by
rbagnall
★ 1.8k
1
vote
1
reply
5.0k
views
Comment:
Comment: EIGENSOFT : Ploteig, 3D Plots
updated 16 months ago by
Ram
43k • written 8.8 years ago by
rbagnall
★ 1.8k
0
votes
2
replies
2.5k
views
Comment:
C: Is there software that takes advantage of MarkedDuplicates for SNP calling?
9.0 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
2.9k
views
Comment:
Comment: Block break from gVCF files
updated 23 months ago by
Ram
43k • written 9.1 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
2.9k
views
Comment:
C: Block break from gVCF files
9.1 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
6.5k
views
Comment:
Comment: GATK: RealignerTargetCreator and IndelRealigner related questions
updated 2.1 years ago by
Ram
43k • written 9.3 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
5.8k
views
Comment:
Comment: Free HiSeq X Ten human genome fastq test data
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
rbagnall
★ 1.8k
0
votes
0
replies
2.5k
views
Comment:
C: Illumina Custom amplicon data issue
9.9 years ago by
rbagnall
★ 1.8k
0
votes
1
reply
4.7k
views
Comment:
C: Variant Annotation, Analysis and Search Tool - VAAST2
10.0 years ago by
rbagnall
★ 1.8k
49 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