Latest
Open
RNA-Seq
ChIP-Seq
SNP
Assembly
Tutorials
Tools
Jobs
Forum
Planet
All »
Home
Log In
Showing: indel • reset
or   Classic search
<prev • 205 results • page 1 of 7 • next >
0
votes
1
answer
130
views
1
answer
Validation of SNP and INDEL calling pipeline
genome indel alignment snp written 8 days ago by kspata • 50 • updated 8 days ago by WouterDeCoster ♦ 39k
0
votes
0
answers
123
views
0
answers
VARIANT effect retrieving
indel variant effect snv written 12 weeks ago by cocchi.e89 • 20 • updated 23 days ago by Biostar ♦♦ 20
3
votes
0
answers
2.2k
views
0
answers
Reducing False Positive Indel Calls From Pindel
indel somatic variant pindel written 7.5 years ago by Rlong • 340 • updated 5 weeks ago by isaacpei • 0
0
votes
1
answer
156
views
1
answer
VCF - InDels and SNPs relation
indel vcf snp written 5 weeks ago by bwczech • 70 • updated 5 weeks ago by Pierre Lindenbaum ♦ 120k
4
votes
3
answers
126
views
3
answers
Finding if dbSNP type in biomart
indel R biomart snp written 5 weeks ago by zakkaknadine • 10 • updated 5 weeks ago by zx8754 ♦ 7.5k
4
votes
1
answer
769
views
1
answer
Identify homopolymer stretches in a given genome
variant calling indel homopolymers snp written 19 months ago by ATpoint ♦ 17k
0
votes
0
answers
85
views
0
answers
difference between Copy Number 0 and INDEL 1000genomes
1000g indel cnv sv written 8 weeks ago by cocchi.e89 • 20
5
votes
1
answer
1.3k
views
1
answer
What Do You Do With Indels Data?
indel analysis written 7.2 years ago by User 2005 • 70 • updated 10 weeks ago by Biostar ♦♦ 20
0
votes
0
answers
1.7k
views
0
answers
Strange variant call it show a indel but looks like a SNP
indel snp variant ion caller written 4.7 years ago by cristianrohr768 • 30 • updated 11 weeks ago by Biostar ♦♦ 20
5
votes
1
answer
211
views
1
answer
New Variants Effect Prediction Tools
indel variant effect snv written 12 weeks ago by cocchi.e89 • 20 • updated 11 weeks ago by Emily_Ensembl ♦ 18k
1
vote
1
answer
403
views
1
answer
RNA-SEQ SNP calling
indel variant snp rna-seq written 4 months ago by babji2318 • 0 • updated 4 months ago by JC ♦ 7.9k
5
votes
5
answers
939
views
5
answers
VariantCalling with single sanger read
indel snps variantcalling blast written 2.8 years ago by Amirosein • 70 • updated 4 months ago by trausch • 1.3k
0
votes
0
answers
187
views
0
answers
how to change indel to smallest length in vcf
indel annotation next-gen vcf written 5 months ago by 1097049297 • 0
8
votes
3
answers
2.9k
views
9 follow
3
answers
Mismatch and Indel statistics from BAM/SAM file
indel bam sam written 2.1 years ago by sbdk82 • 40 • updated 6 months ago by FatihSarigol • 120
7
votes
1
answer
446
views
1
answer
How to merge vcf files (output of VarScan2 somatic)?
vcf indel merge varscan2 snp written 6 months ago by Raheleh • 70
3
votes
1
answer
428
views
1
answer
Variants calling by bcftools
indel alignment snp written 6 months ago by Mbillah • 110 • updated 6 months ago by ATpoint ♦ 17k
2
votes
0
answers
254
views
0
answers
Advice for indel calling
indel rna-seq written 8 months ago by jparker4 • 20 • updated 7 months ago by Biostar ♦♦ 20
1
vote
1
answer
848
views
1
answer
is DANN capable of scoring insertion and deletion?
indel genome annotation snp non-coding written 2.3 years ago by fetus0000 • 20 • updated 7 months ago by Kevin Blighe ♦ 43k
6
votes
0
answers
591
views
0
answers
Long Reads: Nanopore/ PacBio
indel nanopre cnv snv longreads written 7 months ago by ResearchR • 60
1
vote
0
answers
357
views
0
answers
Question about Base calling for pacbio data
genome indel pacbio snp gatk written 8 months ago by kamel • 10 • updated 8 months ago by Vijay Lakhujani ♦ 4.1k
18
votes
4
answers
3.5k
views
5 follow
4
answers
Indel Detection For 454 Resequencing
indel next-gen sequencing written 8.9 years ago by Daniel Swan ♦ 13k • updated 9 months ago by RamRS ♦ 21k
19
votes
4
answers
7.9k
views
8 follow
4
answers
Indel Left/Right Alignment
indel written 6.2 years ago by sa9 • 800 • updated 9 months ago by hugues.sicotte • 0
0
votes
1
answer
399
views
1
answer
Allele counting tool for a list of known indels from paired end sequencing data
indel pindel sequencing allele counting genotyping written 9 months ago by erfan741 • 30 • updated 9 months ago by btsui • 290
4
votes
3
answers
683
views
5 follow
3
answers
Detecting Homozygous Insertion from Sanger Seq
indel sanger written 10 months ago by justinms • 10 • updated 10 months ago by trausch • 1.3k
0
votes
0
answers
288
views
0
answers
using the docker container of cgpPINDEL
indel wgs snv pindel written 12 months ago by Bogdan • 800 • updated 10 months ago by Biostar ♦♦ 20
11
votes
1
answer
2.5k
views
1
answer
Can´T Find The Snps With Samtools (Only Get Indels)
indel alignment samtools snp written 7.8 years ago by Pilar E. • 90 • updated 11 months ago by Biostar ♦♦ 20
0
votes
0
answers
681
views
0
answers
SNP + INDEL Merging Guidelines
vcf indel snp merging written 12 months ago by QVINTVS_FABIVS_MAXIMVS • 2.2k
9
votes
1
answer
742
views
1
answer
When should you left-align INDELs (and why?)
indel vcf left align written 12 months ago by QVINTVS_FABIVS_MAXIMVS • 2.2k
6
votes
2
answers
371
views
5 follow
2
answers
How do variant callers get genotype info?
variant calling indel snp phasing written 12 months ago by afzm • 20 • updated 12 months ago by Jeremy Leipzig ♦ 18k
0
votes
0
answers
380
views
0
answers
How to analyse mtDNA insertion from NGS data?
indel mtdna ngs written 12 months ago by MatthewP • 110
<prev • 205 results • page 1 of 7 • next >
Recent Votes
Recent Locations • All »
  • United States, just now
  • New York, 4 minutes ago
  • Chicago, IL, USA, 5 minutes ago
  • United Kingdom, 10 minutes ago
  • London, 11 minutes ago
Recent Awards • All »
Recent Replies
Content
Help
Access
Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 910 users visited in the last hour