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Comment:
Comment: What is NCBI Gene ID, where to find it and how to convert to entrez ID?
6 hours ago by
barslmn
★ 1.5k
1
vote
0
replies
352
views
Comment:
Comment: ggsave() bug in ggplot2?
6 hours ago by
barslmn
★ 1.5k
0
votes
1
reply
352
views
Comment:
Comment: ggsave() bug in ggplot2?
9 hours ago by
barslmn
★ 1.5k
0
votes
1
reply
352
views
Comment:
Comment: ggsave() bug in ggplot2?
10 hours ago by
barslmn
★ 1.5k
2
votes
1
reply
270
views
Comment:
Comment: BioInformatics, Software
11 hours ago by
barslmn
★ 1.5k
2
votes
1
reply
114
views
Answer:
Answer: How to calculate kinship matrix table from vcf file
11 hours ago by
barslmn
★ 1.5k
0
votes
0
replies
106
views
Comment:
Comment: bioinformatic analysis protocol performed by CD Genomics
12 hours ago by
barslmn
★ 1.5k
1
vote
1
reply
224
views
Comment:
Comment: Docker Error while running nf-core/rnaseq pipeline
1 day ago by
barslmn
★ 1.5k
0
votes
1
reply
224
views
Comment:
Comment: Docker Error while running nf-core/rnaseq pipeline
1 day ago by
barslmn
★ 1.5k
0
votes
0
replies
354
views
Comment:
Comment: Subset FASTA file using partial matching of headers with list of taxon names
9 days ago by
barslmn
★ 1.5k
0
votes
0
replies
2.0k
views
Comment:
Comment: Error in Adding 1000Genomes Ancestral Allele info: Using VCF tools fill-aa
10 days ago by
barslmn
★ 1.5k
0
votes
1
reply
354
views
Answer:
Answer: Subset FASTA file using partial matching of headers with list of taxon names
10 days ago by
barslmn
★ 1.5k
0
votes
0
replies
1.1k
views
Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
13 days ago by
barslmn
★ 1.5k
0
votes
1
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1.1k
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Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
14 days ago by
barslmn
★ 1.5k
0
votes
1
reply
656
views
Comment:
Comment: Prokka installation - compilation aborted
14 days ago by
barslmn
★ 1.5k
1
vote
1
reply
333
views
Comment:
Comment: How can I update fastq-dump to 3.0.0?
15 days ago by
barslmn
★ 1.5k
1
vote
1
reply
1.1k
views
Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
15 days ago by
barslmn
★ 1.5k
1
vote
1
reply
430
views
Comment:
Comment: how to plot SV(structural variants) from many assemblies of a given locus
15 days ago by
barslmn
★ 1.5k
1
vote
0
replies
176
views
Answer:
Answer: How do you go about grabbing proper genotyping information from dbSNP using entr
23 days ago by
barslmn
★ 1.5k
0
votes
1
reply
168
views
Comment:
Comment: Loop through file to assign alphabets to genefeatures for the read intersects
24 days ago by
barslmn
★ 1.5k
1
vote
1
reply
205
views
Comment:
Comment: Should I use mean to show variations among different studies in meta analysis
24 days ago by
barslmn
★ 1.5k
0
votes
0
replies
287
views
Comment:
Comment: How to split a fastq file to multiples fastq files
5 weeks ago by
barslmn
★ 1.5k
0
votes
0
replies
218
views
Comment:
Comment: How do I integrate GRCh38 CADD v1.6 offline with ANNOVAR?
6 weeks ago by
barslmn
★ 1.5k
2
votes
0
replies
295
views
Comment:
Comment: Change sequence ID in fastq file generated by bcftools mpileup
7 weeks ago by
barslmn
★ 1.5k
0
votes
0
replies
462
views
Comment:
Comment: GFF/GTF file error / featureCounts
7 weeks ago by
barslmn
★ 1.5k
0
votes
1
reply
462
views
Comment:
Comment: GFF/GTF file error / featureCounts
8 weeks ago by
barslmn
★ 1.5k
1
vote
1
reply
462
views
Comment:
Comment: GFF/GTF file error / featureCounts
8 weeks ago by
barslmn
★ 1.5k
0
votes
0
replies
383
views
Comment:
Comment: How can I generate VCF file with two different assembled genome fasta?
8 weeks ago by
barslmn
★ 1.5k
1
vote
0
replies
269
views
Comment:
Comment: How to draw boxplot for hub genes
8 weeks ago by
barslmn
★ 1.5k
0
votes
0
replies
233
views
Comment:
Comment: SKAT iniciation
8 weeks ago by
barslmn
★ 1.5k
3
votes
2
replies
470
views
Answer:
Answer: 1000 genomes hg38 with dbSNP rsid
9 weeks ago by
barslmn
★ 1.5k
1
vote
0
replies
270
views
Comment:
Comment: TSV with multi-allelic sites to VCF
10 weeks ago by
barslmn
★ 1.5k
0
votes
1
reply
465
views
Comment:
Comment: Get Exon Sequence from biomaRt given ENST transcript ID and exon number.
11 weeks ago by
barslmn
★ 1.5k
1
vote
0
replies
242
views
Comment:
Comment: how best to analyze vcf files
12 weeks ago by
barslmn
★ 1.5k
0
votes
0
replies
193
views
Comment:
Comment: Custom Annotaion file
12 weeks ago by
barslmn
★ 1.5k
4
votes
1
reply
1.0k
views
Comment:
Comment: Rust bioinformatics projects ideas
12 weeks ago by
barslmn
★ 1.5k
2
votes
1
reply
836
views
Comment:
Comment: bcftools annotate -a
3 months ago by
barslmn
★ 1.5k
0
votes
0
replies
785
views
Answer:
Answer: Using LiftOver to change genomic build
3 months ago by
barslmn
★ 1.5k
0
votes
0
replies
343
views
Comment:
Comment: Annotating VCF and filtering via annotation
3 months ago by
barslmn
★ 1.5k
0
votes
2
replies
819
views
Comment:
Comment: Use bcftools isec to find denovo mutations
3 months ago by
barslmn
★ 1.5k
0
votes
0
replies
570
views
Answer:
Answer: Error: ##fileformat=VCFv4.2 does not exist
3 months ago by
barslmn
★ 1.5k
1
vote
1
reply
681
views
Answer:
Answer: command line - how to change name of multiple files at the same time
3 months ago by
barslmn
★ 1.5k
0
votes
0
replies
929
views
Comment:
Comment: HTSeq error processing GFF file
3 months ago by
barslmn
★ 1.5k
0
votes
1
reply
929
views
Comment:
Comment: HTSeq error processing GFF file
3 months ago by
barslmn
★ 1.5k
0
votes
1
reply
929
views
Comment:
Comment: HTSeq error processing GFF file
3 months ago by
barslmn
★ 1.5k
1
vote
1
reply
559
views
Comment:
Comment: Python Dictionary of Primer3-py Primer Designs
4 months ago by
barslmn
★ 1.5k
0
votes
0
replies
555
views
Answer:
Answer: Download customized list of human protein sequence
4 months ago by
barslmn
★ 1.5k
1
vote
1
reply
559
views
Answer:
Answer: Python Dictionary of Primer3-py Primer Designs
4 months ago by
barslmn
★ 1.5k
0
votes
1
reply
589
views
Comment:
Comment: Issue with VCF format while using Pharmcat
4 months ago by
barslmn
★ 1.5k
0
votes
0
replies
368
views
Comment:
Comment: Variant effect predictor in ictalurus punctatus
4 months ago by
barslmn
★ 1.5k
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