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Comment: Comment: On retrieving SNPs from dbSNP
21 months ago by barslmn ★ 2.4k
1
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1.7k
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Comment: Comment: Contig labels in BAM off by 1, how do I fix it?
21 months ago by barslmn ★ 2.4k
2
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1
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1.7k
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Answer: Answer: Contig labels in BAM off by 1, how do I fix it?
22 months ago by barslmn ★ 2.4k
1
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1
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1.4k
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Comment: Comment: Centromere hg38
22 months ago by barslmn ★ 2.4k
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0
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485
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Why am I seeing this variants genotype as 1/0?
VCF
22 months ago by barslmn ★ 2.4k
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1
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2.1k
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Comment: Comment: Adapter trimming using fastp
22 months ago by barslmn ★ 2.4k
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0
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4.1k
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Comment: Comment: What is NCBI Gene ID, where to find it and how to convert to entrez ID?
23 months ago by barslmn ★ 2.4k
1
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0
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4.3k
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Comment: Comment: ggsave() bug in ggplot2?
23 months ago by barslmn ★ 2.4k
0
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1
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4.3k
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Comment: Comment: ggsave() bug in ggplot2?
23 months ago by barslmn ★ 2.4k
0
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1
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4.3k
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Comment: Comment: ggsave() bug in ggplot2?
23 months ago by barslmn ★ 2.4k
3
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1
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1.8k
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Comment: Comment: BioInformatics, Software
23 months ago by barslmn ★ 2.4k
2
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1
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1.6k
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Answer: Answer: How to calculate kinship matrix table from vcf file
23 months ago by barslmn ★ 2.4k
1
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0
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774
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Comment: Comment: bioinformatic analysis protocol performed by CD Genomics
23 months ago by barslmn ★ 2.4k
1
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1
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2.6k
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Comment: Comment: Docker Error while running nf-core/rnaseq pipeline
23 months ago by barslmn ★ 2.4k
0
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1
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2.6k
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Comment: Comment: Docker Error while running nf-core/rnaseq pipeline
23 months ago by barslmn ★ 2.4k
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0
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1.7k
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Comment: Comment: Subset FASTA file using partial matching of headers with list of taxon names
23 months ago by barslmn ★ 2.4k
0
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0
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2.7k
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Comment: Comment: Error in Adding 1000Genomes Ancestral Allele info: Using VCF tools fill-aa
23 months ago by barslmn ★ 2.4k
0
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1
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1.7k
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Answer: Answer: Subset FASTA file using partial matching of headers with list of taxon names
23 months ago by barslmn ★ 2.4k
0
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0
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3.0k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
23 months ago by barslmn ★ 2.4k
0
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1
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3.0k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
23 months ago by barslmn ★ 2.4k
0
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1
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3.2k
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Comment: Comment: Prokka installation - compilation aborted
23 months ago by barslmn ★ 2.4k
1
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1
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3.1k
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Comment: Comment: How can I update fastq-dump to 3.0.0?
23 months ago by barslmn ★ 2.4k
1
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1
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3.0k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
23 months ago by barslmn ★ 2.4k
1
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1
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1.2k
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Comment: Comment: how to plot SV(structural variants) from many assemblies of a given locus
23 months ago by barslmn ★ 2.4k
1
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0
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719
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Answer: Answer: How do you go about grabbing proper genotyping information from dbSNP using entr
24 months ago by barslmn ★ 2.4k
0
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1
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662
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Comment: Comment: Loop through file to assign alphabets to genefeatures for the read intersects
24 months ago by barslmn ★ 2.4k
1
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1
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706
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Comment: Comment: Should I use mean to show variations among different studies in meta analysis
24 months ago by barslmn ★ 2.4k
0
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0
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953
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Comment: Comment: How to split a fastq file to multiples fastq files
2.0 years ago by barslmn ★ 2.4k
0
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0
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945
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Comment: Comment: How do I integrate GRCh38 CADD v1.6 offline with ANNOVAR?
2.0 years ago by barslmn ★ 2.4k
2
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0
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768
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Comment: Comment: Change sequence ID in fastq file generated by bcftools mpileup
2.1 years ago by barslmn ★ 2.4k
0
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0
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1.9k
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Comment: Comment: GFF/GTF file error / featureCounts
2.1 years ago by barslmn ★ 2.4k
0
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1
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1.9k
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Comment: Comment: GFF/GTF file error / featureCounts
2.1 years ago by barslmn ★ 2.4k
1
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1
reply
1.9k
views
Comment: Comment: GFF/GTF file error / featureCounts
2.1 years ago by barslmn ★ 2.4k
0
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0
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1.7k
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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
2.1 years ago by barslmn ★ 2.4k
1
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0
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1.2k
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Comment: Comment: How to draw boxplot for hub genes
2.1 years ago by barslmn ★ 2.4k
0
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0
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669
views
Comment: Comment: SKAT iniciation
2.1 years ago by barslmn ★ 2.4k
3
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2
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2.9k
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Answer: Answer: 1000 genomes hg38 with dbSNP rsid
2.1 years ago by barslmn ★ 2.4k
1
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0
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969
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Comment: Comment: TSV with multi-allelic sites to VCF
2.1 years ago by barslmn ★ 2.4k
0
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1
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1.7k
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Comment: Comment: Get Exon Sequence from biomaRt given ENST transcript ID and exon number.
2.1 years ago by barslmn ★ 2.4k
1
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0
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829
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Comment: Comment: how best to analyze vcf files
2.1 years ago by barslmn ★ 2.4k
0
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0
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575
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Comment: Comment: Custom Annotaion file
2.1 years ago by barslmn ★ 2.4k
4
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1
reply
4.2k
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Comment: Comment: Rust bioinformatics projects ideas
2.2 years ago by barslmn ★ 2.4k
2
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1
reply
3.9k
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Comment: Comment: bcftools annotate -a
2.2 years ago by barslmn ★ 2.4k
0
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0
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4.3k
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Answer: Answer: Using LiftOver to change genomic build
2.2 years ago by barslmn ★ 2.4k
0
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0
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753
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Comment: Comment: Annotating VCF and filtering via annotation
2.2 years ago by barslmn ★ 2.4k
0
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2
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2.5k
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Comment: Comment: Use bcftools isec to find denovo mutations
2.2 years ago by barslmn ★ 2.4k
0
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0
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1.7k
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Answer: Answer: Error: ##fileformat=VCFv4.2 does not exist
2.2 years ago by barslmn ★ 2.4k
1
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1
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1.8k
views
Answer: Answer: command line - how to change name of multiple files at the same time
2.2 years ago by barslmn ★ 2.4k
0
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0
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2.1k
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Comment: Comment: HTSeq error processing GFF file
2.2 years ago by barslmn ★ 2.4k
0
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1
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2.1k
views
Comment: Comment: HTSeq error processing GFF file
2.2 years ago by barslmn ★ 2.4k
356 results • Page 3 of 8
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