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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
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1.9k
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Comment: Comment: Calculate the percentage of genomic region covered from the BED file.
2.3 years ago by barslmn ★ 2.5k
6
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1
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1.9k
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Answer: Answer: IGV - is it possible to tell what allele a read is from?
2.3 years ago by barslmn ★ 2.5k
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0
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1.3k
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
2.3 years ago by barslmn ★ 2.5k
0
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1
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1.3k
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
2.3 years ago by barslmn ★ 2.5k
0
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0
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1.3k
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Comment: Comment: GATK not working when clone to VM
2.3 years ago by barslmn ★ 2.5k
0
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0
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875
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Comment: Comment: On retrieving SNPs from dbSNP
2.3 years ago by barslmn ★ 2.5k
1
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0
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2.2k
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Comment: Comment: Contig labels in BAM off by 1, how do I fix it?
2.3 years ago by barslmn ★ 2.5k
2
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1
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2.2k
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Answer: Answer: Contig labels in BAM off by 1, how do I fix it?
2.3 years ago by barslmn ★ 2.5k
1
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1
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2.1k
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Comment: Comment: Centromere hg38
2.3 years ago by barslmn ★ 2.5k
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0
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680
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Why am I seeing this variants genotype as 1/0?
VCF
2.4 years ago by barslmn ★ 2.5k
0
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1
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2.7k
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Comment: Comment: Adapter trimming using fastp
2.4 years ago by barslmn ★ 2.5k
0
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0
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5.1k
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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
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0
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5.8k
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Comment: Comment: ggsave() bug in ggplot2?
2.4 years ago by barslmn ★ 2.5k
0
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1
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5.8k
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Comment: Comment: ggsave() bug in ggplot2?
2.4 years ago by barslmn ★ 2.5k
0
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1
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5.8k
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Comment: Comment: ggsave() bug in ggplot2?
2.4 years ago by barslmn ★ 2.5k
3
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1
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2.3k
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Comment: Comment: BioInformatics, Software
2.4 years ago by barslmn ★ 2.5k
2
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1
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2.1k
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Answer: Answer: How to calculate kinship matrix table from vcf file
2.4 years ago by barslmn ★ 2.5k
1
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0
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984
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Comment: Comment: bioinformatic analysis protocol performed by CD Genomics
2.4 years ago by barslmn ★ 2.5k
1
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1
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3.2k
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Comment: Comment: Docker Error while running nf-core/rnaseq pipeline
2.4 years ago by barslmn ★ 2.5k
0
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1
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3.2k
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Comment: Comment: Docker Error while running nf-core/rnaseq pipeline
2.4 years ago by barslmn ★ 2.5k
0
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0
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2.2k
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Comment: Comment: Subset FASTA file using partial matching of headers with list of taxon names
2.5 years ago by barslmn ★ 2.5k
0
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0
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3.0k
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Comment: Comment: Error in Adding 1000Genomes Ancestral Allele info: Using VCF tools fill-aa
2.5 years ago by barslmn ★ 2.5k
0
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1
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2.2k
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Answer: Answer: Subset FASTA file using partial matching of headers with list of taxon names
2.5 years ago by barslmn ★ 2.5k
0
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0
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4.2k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.5 years ago by barslmn ★ 2.5k
0
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1
reply
4.2k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
2.5 years ago by barslmn ★ 2.5k
0
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1
reply
4.1k
views
Comment: Comment: Prokka installation - compilation aborted
2.5 years ago by barslmn ★ 2.5k
1
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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
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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
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1
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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
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0
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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
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1
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843
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Comment: Comment: Loop through file to assign alphabets to genefeatures for the read intersects
2.5 years ago by barslmn ★ 2.5k
1
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1
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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
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0
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1.2k
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Comment: Comment: How to split a fastq file to multiples fastq files
2.5 years ago by barslmn ★ 2.5k
0
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0
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1.1k
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Comment: Comment: How do I integrate GRCh38 CADD v1.6 offline with ANNOVAR?
2.5 years ago by barslmn ★ 2.5k
2
votes
0
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952
views
Comment: Comment: Change sequence ID in fastq file generated by bcftools mpileup
2.6 years ago by barslmn ★ 2.5k
0
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0
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2.4k
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Comment: Comment: GFF/GTF file error / featureCounts
2.6 years ago by barslmn ★ 2.5k
0
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1
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2.4k
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Comment: Comment: GFF/GTF file error / featureCounts
2.6 years ago by barslmn ★ 2.5k
1
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1
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2.4k
views
Comment: Comment: GFF/GTF file error / featureCounts
2.6 years ago by barslmn ★ 2.5k
0
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0
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2.1k
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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
2.6 years ago by barslmn ★ 2.5k
1
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0
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1.5k
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Comment: Comment: How to draw boxplot for hub genes
2.6 years ago by barslmn ★ 2.5k
0
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0
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797
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Comment: Comment: SKAT iniciation
2.6 years ago by barslmn ★ 2.5k
3
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2
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4.0k
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Answer: Answer: 1000 genomes hg38 with dbSNP rsid
2.6 years ago by barslmn ★ 2.5k
1
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0
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1.2k
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Comment: Comment: TSV with multi-allelic sites to VCF
2.6 years ago by barslmn ★ 2.5k
0
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1
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2.5k
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Comment: Comment: Get Exon Sequence from biomaRt given ENST transcript ID and exon number.
2.6 years ago by barslmn ★ 2.5k
1
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0
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1.1k
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Comment: Comment: how best to analyze vcf files
2.7 years ago by barslmn ★ 2.5k
0
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0
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720
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Comment: Comment: Custom Annotaion file
2.7 years ago by barslmn ★ 2.5k
4
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1
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5.3k
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Comment: Comment: Rust bioinformatics projects ideas
2.7 years ago by barslmn ★ 2.5k
2
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1
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4.5k
views
Comment: Comment: bcftools annotate -a
2.7 years ago by barslmn ★ 2.5k
0
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0
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6.0k
views
Answer: Answer: Using LiftOver to change genomic build
2.7 years ago by barslmn ★ 2.5k
362 results • Page 3 of 8
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