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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
17 months ago by barslmn ★ 2.4k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
17 months ago by barslmn ★ 2.4k
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1
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2.7k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
17 months ago by barslmn ★ 2.4k
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Comment: Comment: help with weird PCA? (vcfR)
17 months ago by barslmn ★ 2.4k
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2.7k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
17 months ago by barslmn ★ 2.4k
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2.7k
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Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
17 months ago by barslmn ★ 2.4k
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1.4k
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Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
17 months ago by barslmn ★ 2.4k
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Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
17 months ago by barslmn ★ 2.4k
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1.1k
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Comment: Comment: Calculating height prediction from PGS
17 months ago by barslmn ★ 2.4k
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1.1k
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Comment: Comment: Confirming called variants
17 months ago by barslmn ★ 2.4k
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Comment: Comment: how can i solve a problem in applying a mutation on protein sequence?
17 months ago by barslmn ★ 2.4k
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1.1k
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Comment: Comment: Confirming called variants
17 months ago by barslmn ★ 2.4k
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1.9k
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Comment: Comment: NGS one-liner to call variants
17 months ago by barslmn ★ 2.4k
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1.9k
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Comment: Comment: NGS one-liner to call variants
17 months ago by barslmn ★ 2.4k
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1.9k
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Comment: Comment: NGS one-liner to call variants
17 months ago by barslmn ★ 2.4k
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2.4k
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Comment: Comment: VEP ensemble docker and plugins
17 months ago by barslmn ★ 2.4k
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1.9k
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Comment: Comment: NGS one-liner to call variants
17 months ago by barslmn ★ 2.4k
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598
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Comment: Comment: Pysam pileup and Rsamtools pileup output discrepancy
17 months ago by barslmn ★ 2.4k
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1.9k
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Blog: NGS one-liner to call variants
shell sequencing
updated 17 months ago by 45k • written 17 months ago by ★ 2.4k
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2.4k
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Comment: Comment: VEP ensemble docker and plugins
17 months ago by barslmn ★ 2.4k
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1
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2.4k
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Comment: Comment: VEP ensemble docker and plugins
updated 17 months ago by 45k • written 17 months ago by ★ 2.4k
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2.4k
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Comment: Comment: VEP ensemble docker and plugins
17 months ago by barslmn ★ 2.4k
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1.2k
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Comment: Comment: FASTQ to BAM to CRAM to FASTQ
17 months ago by barslmn ★ 2.4k
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2.2k
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Comment: Comment: Want to check bam file quality
17 months ago by barslmn ★ 2.4k
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886
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Answer: Answer: Commands to do the following in BCFtools or recommendations for another tool
18 months ago by barslmn ★ 2.4k
1
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1
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662
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Comment: Comment: extract first and last n bp from fasta file from multiple fasta file in R
18 months ago by barslmn ★ 2.4k
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1.9k
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Comment: Comment: Troubles launch IGV on Linux(Debian)
18 months ago by barslmn ★ 2.4k
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0
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765
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Comment: Comment: Splitting VCF/BCF file into seperate gene files
18 months ago by barslmn ★ 2.4k
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1
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1.9k
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Answer: Answer: Troubles launch IGV on Linux(Debian)
18 months ago by barslmn ★ 2.4k
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1
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1.9k
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Comment: Comment: Troubles launch IGV on Linux(Debian)
18 months ago by barslmn ★ 2.4k
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1.3k
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Comment: Comment: BED files
18 months ago by barslmn ★ 2.4k
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566
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Comment: Comment: Merging the filename with tsv files for master file
18 months ago by barslmn ★ 2.4k
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0
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589
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Comment: Comment: Download an example of fully-imputed VCF files ?
18 months ago by barslmn ★ 2.4k
1
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1
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960
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Answer: Answer: Fetch genomic region(s) from refseq genomes
19 months ago by barslmn ★ 2.4k
2
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1.7k
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Answer: Answer: What is the common practice to view WGS data on IGV?
19 months ago by barslmn ★ 2.4k
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2.9k
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Comment: Comment: Converting custom VCF to standard VCF
19 months ago by barslmn ★ 2.4k
1
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0
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2.9k
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Answer: Answer: Converting custom VCF to standard VCF
19 months ago by barslmn ★ 2.4k
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2.1k
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Comment: Comment: How to deal with duplicates between two database IDs?
19 months ago by barslmn ★ 2.4k
0
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1
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2.1k
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Answer: Answer: How to deal with duplicates between two database IDs?
19 months ago by barslmn ★ 2.4k
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1
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2.0k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
19 months ago by barslmn ★ 2.4k
2
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1
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2.0k
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Answer: Answer: Tool to search for missing genes among genome annotation versions?
20 months ago by barslmn ★ 2.4k
1
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0
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840
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Answer: Answer: Annotate VCF with RepeatMasker
20 months ago by barslmn ★ 2.4k
7
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0
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768
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Tutorial: Polygenic Risk Score Calculation
genetic-burden r prs ggplot glm
19 months ago by barslmn ★ 2.4k
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0
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1.6k
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Comment: Comment: how to change the 'bcftools plugin' temp directory
20 months ago by barslmn ★ 2.4k
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1
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1.6k
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Comment: Comment: how to change the 'bcftools plugin' temp directory
20 months ago by barslmn ★ 2.4k
1
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0
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1.5k
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Comment: Comment: Calculate the percentage of genomic region covered from the BED file.
20 months ago by barslmn ★ 2.4k
6
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1
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1.4k
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Answer: Answer: IGV - is it possible to tell what allele a read is from?
20 months ago by barslmn ★ 2.4k
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0
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1.0k
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
20 months ago by barslmn ★ 2.4k
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1
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1.0k
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
20 months ago by barslmn ★ 2.4k
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0
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1.0k
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Comment: Comment: GATK not working when clone to VM
20 months ago by barslmn ★ 2.4k
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