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Comment:
Comment: how to change the 'bcftools plugin' temp directory
2.2 years ago by
barslmn
★ 2.5k
1
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0
replies
1.9k
views
Comment:
Comment: Calculate the percentage of genomic region covered from the BED file.
2.3 years ago by
barslmn
★ 2.5k
6
votes
1
reply
1.9k
views
Answer:
Answer: IGV - is it possible to tell what allele a read is from?
2.3 years ago by
barslmn
★ 2.5k
0
votes
0
replies
1.3k
views
Comment:
Comment: How to read Varscan VCF output in column "Cons"?
2.3 years ago by
barslmn
★ 2.5k
0
votes
1
reply
1.3k
views
Comment:
Comment: How to read Varscan VCF output in column "Cons"?
2.3 years ago by
barslmn
★ 2.5k
0
votes
0
replies
1.3k
views
Comment:
Comment: GATK not working when clone to VM
2.3 years ago by
barslmn
★ 2.5k
0
votes
0
replies
875
views
Comment:
Comment: On retrieving SNPs from dbSNP
2.3 years ago by
barslmn
★ 2.5k
1
vote
0
replies
2.2k
views
Comment:
Comment: Contig labels in BAM off by 1, how do I fix it?
2.3 years ago by
barslmn
★ 2.5k
2
votes
1
reply
2.2k
views
Answer:
Answer: Contig labels in BAM off by 1, how do I fix it?
2.3 years ago by
barslmn
★ 2.5k
1
vote
1
reply
2.1k
views
Comment:
Comment: Centromere hg38
2.3 years ago by
barslmn
★ 2.5k
0
votes
0
replies
680
views
Why am I seeing this variants genotype as 1/0?
VCF
2.4 years ago by
barslmn
★ 2.5k
0
votes
1
reply
2.7k
views
Comment:
Comment: Adapter trimming using fastp
2.4 years ago by
barslmn
★ 2.5k
0
votes
0
replies
5.1k
views
Comment:
Comment: What is NCBI Gene ID, where to find it and how to convert to entrez ID?
2.4 years ago by
barslmn
★ 2.5k
1
vote
0
replies
5.8k
views
Comment:
Comment: ggsave() bug in ggplot2?
2.4 years ago by
barslmn
★ 2.5k
0
votes
1
reply
5.8k
views
Comment:
Comment: ggsave() bug in ggplot2?
2.4 years ago by
barslmn
★ 2.5k
0
votes
1
reply
5.8k
views
Comment:
Comment: ggsave() bug in ggplot2?
2.4 years ago by
barslmn
★ 2.5k
3
votes
1
reply
2.3k
views
Comment:
Comment: BioInformatics, Software
2.4 years ago by
barslmn
★ 2.5k
2
votes
1
reply
2.1k
views
Answer:
Answer: How to calculate kinship matrix table from vcf file
2.4 years ago by
barslmn
★ 2.5k
1
vote
0
replies
984
views
Comment:
Comment: bioinformatic analysis protocol performed by CD Genomics
2.4 years ago by
barslmn
★ 2.5k
1
vote
1
reply
3.2k
views
Comment:
Comment: Docker Error while running nf-core/rnaseq pipeline
2.4 years ago by
barslmn
★ 2.5k
0
votes
1
reply
3.2k
views
Comment:
Comment: Docker Error while running nf-core/rnaseq pipeline
2.4 years ago by
barslmn
★ 2.5k
0
votes
0
replies
2.2k
views
Comment:
Comment: Subset FASTA file using partial matching of headers with list of taxon names
2.5 years ago by
barslmn
★ 2.5k
0
votes
0
replies
3.0k
views
Comment:
Comment: Error in Adding 1000Genomes Ancestral Allele info: Using VCF tools fill-aa
2.5 years ago by
barslmn
★ 2.5k
0
votes
1
reply
2.2k
views
Answer:
Answer: Subset FASTA file using partial matching of headers with list of taxon names
2.5 years ago by
barslmn
★ 2.5k
0
votes
0
replies
4.2k
views
Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.5 years ago by
barslmn
★ 2.5k
0
votes
1
reply
4.2k
views
Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.5 years ago by
barslmn
★ 2.5k
0
votes
1
reply
4.1k
views
Comment:
Comment: Prokka installation - compilation aborted
2.5 years ago by
barslmn
★ 2.5k
1
vote
1
reply
4.0k
views
Comment:
Comment: How can I update fastq-dump to 3.0.0?
2.5 years ago by
barslmn
★ 2.5k
1
vote
1
reply
4.2k
views
Comment:
Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.5 years ago by
barslmn
★ 2.5k
1
vote
1
reply
1.5k
views
Comment:
Comment: how to plot SV(structural variants) from many assemblies of a given locus
2.5 years ago by
barslmn
★ 2.5k
1
vote
0
replies
990
views
Answer:
Answer: How do you go about grabbing proper genotyping information from dbSNP using entr
2.5 years ago by
barslmn
★ 2.5k
0
votes
1
reply
843
views
Comment:
Comment: Loop through file to assign alphabets to genefeatures for the read intersects
2.5 years ago by
barslmn
★ 2.5k
1
vote
1
reply
888
views
Comment:
Comment: Should I use mean to show variations among different studies in meta analysis
2.5 years ago by
barslmn
★ 2.5k
0
votes
0
replies
1.2k
views
Comment:
Comment: How to split a fastq file to multiples fastq files
2.5 years ago by
barslmn
★ 2.5k
0
votes
0
replies
1.1k
views
Comment:
Comment: How do I integrate GRCh38 CADD v1.6 offline with ANNOVAR?
2.5 years ago by
barslmn
★ 2.5k
2
votes
0
replies
952
views
Comment:
Comment: Change sequence ID in fastq file generated by bcftools mpileup
2.6 years ago by
barslmn
★ 2.5k
0
votes
0
replies
2.4k
views
Comment:
Comment: GFF/GTF file error / featureCounts
2.6 years ago by
barslmn
★ 2.5k
0
votes
1
reply
2.4k
views
Comment:
Comment: GFF/GTF file error / featureCounts
2.6 years ago by
barslmn
★ 2.5k
1
vote
1
reply
2.4k
views
Comment:
Comment: GFF/GTF file error / featureCounts
2.6 years ago by
barslmn
★ 2.5k
0
votes
0
replies
2.1k
views
Comment:
Comment: How can I generate VCF file with two different assembled genome fasta?
2.6 years ago by
barslmn
★ 2.5k
1
vote
0
replies
1.5k
views
Comment:
Comment: How to draw boxplot for hub genes
2.6 years ago by
barslmn
★ 2.5k
0
votes
0
replies
797
views
Comment:
Comment: SKAT iniciation
2.6 years ago by
barslmn
★ 2.5k
3
votes
2
replies
4.0k
views
Answer:
Answer: 1000 genomes hg38 with dbSNP rsid
2.6 years ago by
barslmn
★ 2.5k
1
vote
0
replies
1.2k
views
Comment:
Comment: TSV with multi-allelic sites to VCF
2.6 years ago by
barslmn
★ 2.5k
0
votes
1
reply
2.5k
views
Comment:
Comment: Get Exon Sequence from biomaRt given ENST transcript ID and exon number.
2.6 years ago by
barslmn
★ 2.5k
1
vote
0
replies
1.1k
views
Comment:
Comment: how best to analyze vcf files
2.7 years ago by
barslmn
★ 2.5k
0
votes
0
replies
720
views
Comment:
Comment: Custom Annotaion file
2.7 years ago by
barslmn
★ 2.5k
4
votes
1
reply
5.3k
views
Comment:
Comment: Rust bioinformatics projects ideas
2.7 years ago by
barslmn
★ 2.5k
2
votes
1
reply
4.5k
views
Comment:
Comment: bcftools annotate -a
2.7 years ago by
barslmn
★ 2.5k
0
votes
0
replies
6.0k
views
Answer:
Answer: Using LiftOver to change genomic build
2.7 years ago by
barslmn
★ 2.5k
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