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Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
12 months ago by barslmn ★ 2.3k
2
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1
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894
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Comment: Comment: Calculating height prediction from PGS
13 months ago by barslmn ★ 2.3k
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886
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Comment: Comment: Confirming called variants
13 months ago by barslmn ★ 2.3k
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1
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1.0k
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Comment: Comment: how can i solve a problem in applying a mutation on protein sequence?
13 months ago by barslmn ★ 2.3k
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1
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886
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Comment: Comment: Confirming called variants
13 months ago by barslmn ★ 2.3k
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1.6k
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Comment: Comment: NGS one-liner to call variants
13 months ago by barslmn ★ 2.3k
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1.6k
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Comment: Comment: NGS one-liner to call variants
13 months ago by barslmn ★ 2.3k
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1
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1.6k
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Comment: Comment: NGS one-liner to call variants
13 months ago by barslmn ★ 2.3k
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1.9k
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Comment: Comment: VEP ensemble docker and plugins
13 months ago by barslmn ★ 2.3k
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1.6k
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Comment: Comment: NGS one-liner to call variants
13 months ago by barslmn ★ 2.3k
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0
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491
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Comment: Comment: Pysam pileup and Rsamtools pileup output discrepancy
13 months ago by barslmn ★ 2.3k
16
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9
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1.6k
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Blog: NGS one-liner to call variants
shell sequencing
updated 13 months ago by 44k • written 13 months ago by ★ 2.3k
0
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1
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1.9k
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Comment: Comment: VEP ensemble docker and plugins
13 months ago by barslmn ★ 2.3k
0
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1
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1.9k
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Comment: Comment: VEP ensemble docker and plugins
updated 13 months ago by 44k • written 13 months ago by ★ 2.3k
0
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1
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1.9k
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Comment: Comment: VEP ensemble docker and plugins
13 months ago by barslmn ★ 2.3k
1
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1.0k
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Comment: Comment: FASTQ to BAM to CRAM to FASTQ
13 months ago by barslmn ★ 2.3k
1
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1.5k
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Comment: Comment: Want to check bam file quality
13 months ago by barslmn ★ 2.3k
1
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0
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705
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Answer: Answer: Commands to do the following in BCFtools or recommendations for another tool
13 months ago by barslmn ★ 2.3k
1
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1
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541
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Comment: Comment: extract first and last n bp from fasta file from multiple fasta file in R
13 months ago by barslmn ★ 2.3k
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1.6k
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Comment: Comment: Troubles launch IGV on Linux(Debian)
14 months ago by barslmn ★ 2.3k
0
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648
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Comment: Comment: Splitting VCF/BCF file into seperate gene files
14 months ago by barslmn ★ 2.3k
0
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1
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1.6k
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Answer: Answer: Troubles launch IGV on Linux(Debian)
14 months ago by barslmn ★ 2.3k
0
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1
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1.6k
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Comment: Comment: Troubles launch IGV on Linux(Debian)
14 months ago by barslmn ★ 2.3k
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0
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1.0k
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Comment: Comment: BED files
14 months ago by barslmn ★ 2.3k
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482
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Comment: Comment: Merging the filename with tsv files for master file
14 months ago by barslmn ★ 2.3k
0
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486
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Comment: Comment: Download an example of fully-imputed VCF files ?
14 months ago by barslmn ★ 2.3k
1
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1
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801
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Answer: Answer: Fetch genomic region(s) from refseq genomes
15 months ago by barslmn ★ 2.3k
2
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0
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1.4k
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Answer: Answer: What is the common practice to view WGS data on IGV?
15 months ago by barslmn ★ 2.3k
0
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0
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2.3k
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Comment: Comment: Converting custom VCF to standard VCF
15 months ago by barslmn ★ 2.3k
1
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0
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2.3k
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Answer: Answer: Converting custom VCF to standard VCF
15 months ago by barslmn ★ 2.3k
0
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1.7k
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Comment: Comment: How to deal with duplicates between two database IDs?
15 months ago by barslmn ★ 2.3k
0
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1
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1.7k
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Answer: Answer: How to deal with duplicates between two database IDs?
15 months ago by barslmn ★ 2.3k
0
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1
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1.6k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
15 months ago by barslmn ★ 2.3k
2
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1
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1.6k
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Answer: Answer: Tool to search for missing genes among genome annotation versions?
15 months ago by barslmn ★ 2.3k
1
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0
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717
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Answer: Answer: Annotate VCF with RepeatMasker
15 months ago by barslmn ★ 2.3k
7
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0
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703
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Tutorial: Polygenic Risk Score Calculation
genetic-burden r prs ggplot glm
15 months ago by barslmn ★ 2.3k
0
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0
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1.2k
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Comment: Comment: how to change the 'bcftools plugin' temp directory
15 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: how to change the 'bcftools plugin' temp directory
15 months ago by barslmn ★ 2.3k
1
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0
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1.2k
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Comment: Comment: Calculate the percentage of genomic region covered from the BED file.
16 months ago by barslmn ★ 2.3k
6
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1
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1.2k
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Answer: Answer: IGV - is it possible to tell what allele a read is from?
16 months ago by barslmn ★ 2.3k
0
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0
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855
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
16 months ago by barslmn ★ 2.3k
0
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1
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855
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Comment: Comment: How to read Varscan VCF output in column "Cons"?
16 months ago by barslmn ★ 2.3k
0
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0
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841
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Comment: Comment: GATK not working when clone to VM
16 months ago by barslmn ★ 2.3k
0
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0
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547
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Comment: Comment: On retrieving SNPs from dbSNP
16 months ago by barslmn ★ 2.3k
1
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0
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1.3k
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Comment: Comment: Contig labels in BAM off by 1, how do I fix it?
16 months ago by barslmn ★ 2.3k
2
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1
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1.3k
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Answer: Answer: Contig labels in BAM off by 1, how do I fix it?
16 months ago by barslmn ★ 2.3k
1
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1
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1.1k
views
Comment: Comment: Centromere hg38
16 months ago by barslmn ★ 2.3k
0
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0
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435
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Why am I seeing this variants genotype as 1/0?
VCF
17 months ago by barslmn ★ 2.3k
0
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1
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1.7k
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Comment: Comment: Adapter trimming using fastp
17 months ago by barslmn ★ 2.3k
0
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0
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3.5k
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Comment: Comment: What is NCBI Gene ID, where to find it and how to convert to entrez ID?
18 months ago by barslmn ★ 2.3k
349 results • Page 2 of 7
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