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
321
views
Comment:
Comment: What can cause broken read-pairs (chimeric read-pairs) in a sequencing run?
7 weeks ago by
William
★ 5.2k
0
votes
0
replies
321
views
Comment:
Comment: What can cause broken read-pairs (chimeric read-pairs) in a sequencing run?
7 weeks ago by
William
★ 5.2k
0
votes
1
reply
351
views
Comment:
Comment: Difference between mRNA and transcript record types in GFF3 and GTF
8 weeks ago by
William
★ 5.2k
1
vote
2
replies
3.9k
views
Comment:
Comment: Is there a file format better suited for the era of pangenomics than the .vcf? W
9 months ago by
William
★ 5.2k
1
vote
0
replies
627
views
Comment:
Comment: Reduce poly-N regions longer than 200bp back to 200bp in a reference genome FAST
12 months ago by
William
★ 5.2k
0
votes
1
reply
627
views
Comment:
Comment: Reduce poly-N regions longer than 200bp back to 200bp in a reference genome FAST
12 months ago by
William
★ 5.2k
0
votes
1
reply
956
views
Comment:
Comment: How to convert VCF (with possible predicted gene effects) to protein fasta/MSA
14 months ago by
William
★ 5.2k
0
votes
0
replies
737
views
Comment:
Comment: How to estimate and visualize haplotype blocks on a phased VCF/BCF
14 months ago by
William
★ 5.2k
0
votes
0
replies
1.1k
views
Comment:
Comment: how to calculate %of missing genotype in vcf file
18 months ago by
William
★ 5.2k
1
vote
0
replies
1.6k
views
Comment:
Comment: Is it possible to construct a full genome from whole sequence VCF files containi
2.5 years ago by
William
★ 5.2k
0
votes
0
replies
1.3k
views
Comment:
Comment: Merging VCF files.
2.5 years ago by
William
★ 5.2k
0
votes
1
reply
1.4k
views
Comment:
Comment: Strange speed up in GATK LeftAlignIndels
2.5 years ago by
William
★ 5.2k
0
votes
0
replies
2.5k
views
Comment:
Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
2.5 years ago by
William
★ 5.2k
0
votes
0
replies
2.5k
views
Comment:
Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
2.5 years ago by
William
★ 5.2k
0
votes
1
reply
2.5k
views
Comment:
Comment: User friendly (visual&interactive) VCF/BCF mining tools (2021)
2.5 years ago by
William
★ 5.2k
0
votes
0
replies
3.4k
views
Comment:
Comment: How to set variant FILTER in a VCF file based on overlap with regions in a BED
2.6 years ago by
William
★ 5.2k
0
votes
0
replies
867
views
Comment:
Comment: Wobbly average GC profile spanning entire read length; what the cause and is it
2.8 years ago by
William
★ 5.2k
0
votes
0
replies
1.2k
views
Comment:
Comment: Best pre and post alignment / variant calling QC tools for many WGS/RNA samples
2.8 years ago by
William
★ 5.2k
0
votes
1
reply
3.3k
views
Comment:
Comment: 2021: state and usuge of compressed file standards better than BAM and FASTQ
2.9 years ago by
William
★ 5.2k
0
votes
1
reply
3.3k
views
Comment:
Comment: 2021: state and usuge of compressed file standards better than BAM and FASTQ
2.9 years ago by
William
★ 5.2k
0
votes
1
reply
3.3k
views
Comment:
Comment: 2021: state and usuge of compressed file standards better than BAM and FASTQ
2.9 years ago by
William
★ 5.2k
0
votes
0
replies
1.3k
views
Comment:
C: Best (GATK compatible) RadSeq/GBS pipeline in 2021
3.0 years ago by
William
★ 5.2k
0
votes
0
replies
2.0k
views
Comment:
C: How to convert a VCF with genotypes and phasing info to list of haplotypes for R
3.2 years ago by
William
★ 5.2k
1
vote
0
replies
2.8k
views
Comment:
C: How to filter a gff3 file by gene IDs
3.2 years ago by
William
★ 5.2k
0
votes
0
replies
2.8k
views
Comment:
C: How to filter a gff3 file by gene IDs
3.2 years ago by
William
★ 5.2k
0
votes
1
reply
2.8k
views
Comment:
C: How to filter a gff3 file by gene IDs
3.3 years ago by
William
★ 5.2k
0
votes
0
replies
757
views
Comment:
C: Count all (non N) nucleotides within regions defined in BED file
3.3 years ago by
William
★ 5.2k
0
votes
0
replies
1.4k
views
Comment:
C: Best way to find intervals for parallelization of joint variant calling
3.3 years ago by
William
★ 5.2k
0
votes
1
reply
1.4k
views
Comment:
C: Best way to find intervals for parallelization of joint variant calling
3.3 years ago by
William
★ 5.2k
0
votes
2
replies
4.0k
views
Comment:
C: Sort gff3 on chromosome, position and then featuretype (gene, mRNA, exon, CDS)
3.9 years ago by
William
★ 5.2k
0
votes
1
reply
4.0k
views
Comment:
C: Sort gff3 on chromosome, position and then featuretype (gene, mRNA, exon, CDS)
3.9 years ago by
William
★ 5.2k
0
votes
1
reply
4.0k
views
Comment:
C: Sort gff3 on chromosome, position and then featuretype (gene, mRNA, exon, CDS)
3.9 years ago by
William
★ 5.2k
0
votes
1
reply
3.7k
views
Comment:
C: Breakdancer Compile Error: Regionlimitedbamreader.Hpp:23:5: Error: ‘Bam_Iter_T’
updated 4.5 years ago by
Ram
43k • written 10.6 years ago by
William
★ 5.2k
1
vote
0
replies
17k
views
Comment:
C: Combine Single Sample Vcf To Multi Sample Vcf
updated 5.2 years ago by
Ram
43k • written 10.8 years ago by
William
★ 5.2k
0
votes
0
replies
4.5k
views
Comment:
C: Difference between . and ./. for missing genotype in VCF
5.4 years ago by
William
★ 5.2k
0
votes
0
replies
3.2k
views
Comment:
C: How to do SNP selection in large VCF/BCF/GenotypeTables in R like you can using
6.0 years ago by
William
★ 5.2k
0
votes
0
replies
3.2k
views
Comment:
C: How to do SNP selection in large VCF/BCF/GenotypeTables in R like you can using
6.0 years ago by
William
★ 5.2k
0
votes
1
reply
3.2k
views
Comment:
C: How to do SNP selection in large VCF/BCF/GenotypeTables in R like you can using
6.0 years ago by
William
★ 5.2k
0
votes
1
reply
3.2k
views
Comment:
C: How to do SNP selection in large VCF/BCF/GenotypeTables in R like you can using
6.0 years ago by
William
★ 5.2k
0
votes
1
reply
3.2k
views
Comment:
C: How to do SNP selection in large VCF/BCF/GenotypeTables in R like you can using
6.0 years ago by
William
★ 5.2k
0
votes
1
reply
3.2k
views
Comment:
C: Sensitive (BLAST like) and fast alignment of millions of sequences against human
6.1 years ago by
William
★ 5.2k
0
votes
1
reply
3.2k
views
Comment:
C: Sensitive (BLAST like) and fast alignment of millions of sequences against human
6.1 years ago by
William
★ 5.2k
0
votes
0
replies
3.2k
views
Comment:
C: Sensitive (BLAST like) and fast alignment of millions of sequences against human
6.1 years ago by
William
★ 5.2k
0
votes
1
reply
2.2k
views
Comment:
C: Should I use a bad/ mediocre gene model as input for STAR RNA-seq alignment?
6.2 years ago by
William
★ 5.2k
0
votes
1
reply
2.6k
views
Comment:
C: How to display a VCF/BCF file or stream as a paginated table in a python web fra
6.4 years ago by
William
★ 5.2k
0
votes
0
replies
2.6k
views
Comment:
C: How to display a VCF/BCF file or stream as a paginated table in a python web fra
6.4 years ago by
William
★ 5.2k
0
votes
0
replies
2.3k
views
Comment:
C: Is it possible to use haplotypes instead of SNPs for association testing with ph
6.6 years ago by
William
★ 5.2k
0
votes
0
replies
2.3k
views
Comment:
C: Is it possible to use haplotypes instead of SNPs for association testing with ph
6.6 years ago by
William
★ 5.2k
0
votes
0
replies
3.6k
views
Comment:
C: Python library for parsing bcftools stats file
6.7 years ago by
William
★ 5.2k
0
votes
0
replies
4.9k
views
Comment:
C: CombineGVCFs + GenotypeGVCFs for Freebayes gVCF files?
7.1 years ago by
William
★ 5.2k
139 results • Page
1 of 3
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