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3
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412
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
7 weeks ago by barslmn ★ 2.2k
0
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1
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517
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Answer: Answer: Development plan for a bioinformatics database developer/coder
9 weeks ago by barslmn ★ 2.2k
1
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0
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372
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Answer: Answer: Nextflow crash on AWS Batch with transition error
10 weeks ago by barslmn ★ 2.2k
1
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0
replies
599
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Answer: Answer: split sequences into their codons in a table
4 months ago by barslmn ★ 2.2k
0
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0
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913
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Answer: Answer: How to rename multiple fasq files
4 months ago by barslmn ★ 2.2k
0
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1
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549
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
6 months ago by barslmn ★ 2.2k
1
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1
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1.4k
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Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
1
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0
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971
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Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
6 months ago by barslmn ★ 2.2k
1
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0
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538
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Answer: Answer: Commands to do the following in BCFtools or recommendations for another tool
7 months ago by barslmn ★ 2.2k
0
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1
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1.1k
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Answer: Answer: Troubles launch IGV on Linux(Debian)
7 months ago by barslmn ★ 2.2k
1
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1
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650
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Answer: Answer: Fetch genomic region(s) from refseq genomes
8 months ago by barslmn ★ 2.2k
2
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0
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1.1k
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Answer: Answer: What is the common practice to view WGS data on IGV?
8 months ago by barslmn ★ 2.2k
1
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0
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1.6k
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Answer: Answer: Converting custom VCF to standard VCF
8 months ago by barslmn ★ 2.2k
0
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1
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1.3k
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Answer: Answer: How to deal with duplicates between two database IDs?
9 months ago by barslmn ★ 2.2k
2
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1
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1.2k
views
Answer: Answer: Tool to search for missing genes among genome annotation versions?
9 months ago by barslmn ★ 2.2k
1
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0
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557
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Answer: Answer: Annotate VCF with RepeatMasker
9 months ago by barslmn ★ 2.2k
6
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1
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891
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Answer: Answer: IGV - is it possible to tell what allele a read is from?
9 months ago by barslmn ★ 2.2k
2
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1
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1.0k
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Answer: Answer: Contig labels in BAM off by 1, how do I fix it?
10 months ago by barslmn ★ 2.2k
2
votes
1
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937
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Answer: Answer: How to calculate kinship matrix table from vcf file
11 months ago by barslmn ★ 2.2k
0
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1
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1.1k
views
Answer: Answer: Subset FASTA file using partial matching of headers with list of taxon names
12 months ago by barslmn ★ 2.2k
1
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0
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462
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Answer: Answer: How do you go about grabbing proper genotyping information from dbSNP using entr
12 months ago by barslmn ★ 2.2k
3
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2
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1.7k
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Answer: Answer: 1000 genomes hg38 with dbSNP rsid
13 months ago by barslmn ★ 2.2k
0
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0
replies
2.2k
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Answer: Answer: Using LiftOver to change genomic build
15 months ago by barslmn ★ 2.2k
0
votes
0
replies
1.1k
views
Answer: Answer: Error: ##fileformat=VCFv4.2 does not exist
15 months ago by barslmn ★ 2.2k
1
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1
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1.2k
views
Answer: Answer: command line - how to change name of multiple files at the same time
15 months ago by barslmn ★ 2.2k
0
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0
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1.3k
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Answer: Answer: Download customized list of human protein sequence
15 months ago by barslmn ★ 2.2k
1
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1
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1.0k
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Answer: Answer: Python Dictionary of Primer3-py Primer Designs
15 months ago by barslmn ★ 2.2k
2
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1
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705
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Answer: Answer: Annotating snps with gene information
15 months ago by barslmn ★ 2.2k
1
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1
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818
views
Answer: Answer: How can I construct the adjacency matrix for gene ontology between genes
15 months ago by barslmn ★ 2.2k
1
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1
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975
views
Answer: Answer: Bedtools give different output
16 months ago by barslmn ★ 2.2k
0
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0
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809
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Answer: Answer: GO ontology
16 months ago by barslmn ★ 2.2k
2
votes
1
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680
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Answer: Answer: Looking for list(s) of human genes which are differentially expressed between ma
16 months ago by barslmn ★ 2.2k
0
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1
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604
views
Answer: Answer: Visualization of Pedigree reconstruction
16 months ago by barslmn ★ 2.2k
0
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0
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1.4k
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Answer: Answer: Does a merged VCF file (using bcftools merge) contain unique SNPs or INDELs fro
16 months ago by barslmn ★ 2.2k
3
votes
1
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684
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Answer: Answer: limiting functions to some columns in r
16 months ago by barslmn ★ 2.2k
3
votes
1
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1.3k
views
Answer: Answer: bowtie2, and python script
16 months ago by barslmn ★ 2.2k
2
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0
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1.9k
views
Answer: Answer: speeding up bcftools view
16 months ago by barslmn ★ 2.2k
2
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1
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1.0k
views
Answer: Answer: CAAD score for SNPs vcf file
16 months ago by barslmn ★ 2.2k
0
votes
1
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1.1k
views
Answer: Answer: Where to download the MAF database from 1000 genomes? ANNOVAR looks incomplete
16 months ago by barslmn ★ 2.2k
1
vote
0
replies
514
views
Answer: Answer: Bash script for checking multi variable in if and for loop
16 months ago by barslmn ★ 2.2k
1
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1
reply
1.4k
views
Answer: Answer: Any command line tools that can design primers from a multiple sequence alignmen
16 months ago by barslmn ★ 2.2k
1
vote
0
replies
577
views
Answer: Answer: is it mandatory to use fixmate?
16 months ago by barslmn ★ 2.2k
2
votes
1
reply
755
views
Answer: Answer: how the thickness of the line can be changed in the plotAvgProf ?
16 months ago by barslmn ★ 2.2k
1
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1
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1.0k
views
Answer: Answer: Markduplicate error in picard
16 months ago by barslmn ★ 2.2k
1
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0
replies
1.5k
views
Answer: Answer: How to get transcriptome reference?
16 months ago by barslmn ★ 2.2k
2
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1
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2.0k
views
Answer: Answer: How to Diagnose Fragile X from Whole Genome Sequencing
16 months ago by barslmn ★ 2.2k
0
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0
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6.0k
views
Answer: Answer: Downloading from GEO
16 months ago by barslmn ★ 2.2k
1
vote
0
replies
498
views
Answer: Answer: STAR Alignment Command Error
17 months ago by barslmn ★ 2.2k
4
votes
1
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942
views
Answer: Answer: Making API request to UCSC Genome API for T2T CHM13v2.0/hs1 DNA sequence
17 months ago by barslmn ★ 2.2k
1
vote
0
replies
1.7k
views
Answer: Answer: VEP with CONDA, installing annotation sources manually, what is the right direct
17 months ago by barslmn ★ 2.2k
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