Showing: variationreset
<prev • 60 results • page 1 of 2 • next >
1
vote
0
answers
117
views
0
answers
0
votes
0
answers
144
views
0
answers
0
votes
0
answers
205
views
0
answers
9
votes
1
answer
403
views
1
answer
2
votes
0
answers
1.2k
views
0
answers
Report haplotype frequencies from a region within a phased vcf file
variation haplotype snp written 2.2 years ago by Krisr460 • updated 8 months ago by Biostar ♦♦ 20
1
vote
1
answer
551
views
1
answer
How to Get only one annotation with the SnpEff annotation?
annotation variation snpeff snp written 12 months ago by mhmtgenc8530 • updated 12 months ago by Pierre Lindenbaum121k
2
votes
1
answer
471
views
1
answer
Forum: Theory v Reality
protein forum variation polymorphism dna written 15 months ago by urema0
19
votes
4
answers
4.7k
views
7 follow
4
answers
How To Retrieve Gene Variations From Ensembl Using The Perl Api?
perl ensembl api variation written 8.4 years ago by Jarretinha3.3k • updated 15 months ago by Biostar ♦♦ 20
15
votes
5
answers
6.0k
views
17 follow
5
answers
2
votes
1
answer
1.2k
views
1
answer
How to retrieve COSMIC variations using Ensembl REST API?
ensembl api variation cosmic written 2.5 years ago by patrick.durand120 • updated 2.1 years ago by Biostar ♦♦ 20
0
votes
1
answer
484
views
1
answer
Designating regulatory region threshold
gene ensembl regulation variation promoter written 2.1 years ago by johntimcham0 • updated 2.1 years ago by Emily_Ensembl18k
3
votes
0
answers
611
views
0
answers
Forum: Survey for VEP users
ensembl survey variation vep forum written 2.2 years ago by Emily_Ensembl18k
1
vote
0
answers
1.9k
views
0
answers
How To Tune Parameters When Running Shrimp2 On Longer Illumina Reads
seq variation miseq alignment written 6.5 years ago by kanwarjag970 • updated 2.4 years ago by Biostar ♦♦ 20
3
votes
2
answers
1.9k
views
2
answers
Bcftools equivalent of vcf-merge R?
vcf variation bcftools genotype written 3.3 years ago by CuriousGuy30 • updated 2.5 years ago by Biostar ♦♦ 20
0
votes
0
answers
779
views
0
answers
10
votes
3
answers
3.4k
views
3
answers
Get number of variations in a huge VCF using Tabix?
vcf tabix variation big data written 3.7 years ago by Dan500 • updated 2.8 years ago by Thomas Johnson70
1
vote
1
answer
959
views
1
answer
0
votes
1
answer
789
views
1
answer
3
votes
0
answers
722
views
0
answers
6
votes
1
answer
804
views
1
answer
2
votes
1
answer
940
views
1
answer
chromosomal locations of snps in humvar variant set
variation humvar snp uniprot written 3.2 years ago by arronslacey260 • updated 3.2 years ago by Elisabeth Gasteiger1.6k
2
votes
2
answers
961
views
2
answers
0
votes
1
answer
1.2k
views
1
answer
Targeted resequencing analysis workflow
genome assembly next-gen variation written 4.0 years ago by renjukrishna130 • updated 3.3 years ago by ####190
2
votes
1
answer
875
views
1
answer
Is there any existed tool for retrieving DBsnp from Blast output
variation next-gen alignment dbsnp blast written 3.6 years ago by 30977248660 • updated 3.4 years ago by Benn7.1k
8
votes
1
answer
1.0k
views
1
answer
Genome browser for website (ASP.net)
genome browser variation asp.net snp written 3.5 years ago by Whoknows740 • updated 3.5 years ago by Jean-Karim Heriche20k
1
vote
1
answer
4.1k
views
1
answer
Software For Amova And Population Comparison
population variation written 5.4 years ago by reis.a.rita0 • updated 4.0 years ago by Sabine60
2
votes
0
answers
1.2k
views
0
answers
7
votes
1
answer
4.8k
views
1
answer
2
votes
2
answers
2.1k
views
2
answers
2
votes
1
answer
1.2k
views
1
answer
Illuminia Vs 454 Coverage Spread
illumina variation 454 coverage sequencing written 4.9 years ago by wizard-1410 • updated 4.8 years ago by Biostar ♦♦ 20
<prev • 60 results • page 1 of 2 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 699 users visited in the last hour