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Comment: Comment: NF-Core
21 months ago by barslmn ★ 2.5k
0
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1.8k
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
22 months ago by barslmn ★ 2.5k
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2.0k
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Answer: Answer: How to rename multiple fasq files
22 months ago by barslmn ★ 2.5k
2
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0
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979
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Comment: Comment: unicycler error : [Errno 13] Permission denied:
23 months ago by barslmn ★ 2.5k
0
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0
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784
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Comment: Comment: Python function to export the annotated records to genbank file using python and
23 months ago by barslmn ★ 2.5k
0
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1
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1.8k
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
24 months ago by barslmn ★ 2.5k
0
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0
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3.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
24 months ago by barslmn ★ 2.5k
0
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1
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3.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
24 months ago by barslmn ★ 2.5k
0
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1
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3.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
24 months ago by barslmn ★ 2.5k
0
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1
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1.9k
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Comment: Comment: help with weird PCA? (vcfR)
24 months ago by barslmn ★ 2.5k
0
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1
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3.9k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
24 months ago by barslmn ★ 2.5k
1
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1
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3.9k
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Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
24 months ago by barslmn ★ 2.5k
0
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1
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1.9k
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Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
2.0 years ago by barslmn ★ 2.5k
1
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0
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2.1k
views
Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
2.0 years ago by barslmn ★ 2.5k
2
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1
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1.4k
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Comment: Comment: Calculating height prediction from PGS
2.0 years ago by barslmn ★ 2.5k
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0
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1.4k
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Comment: Comment: Confirming called variants
2.0 years ago by barslmn ★ 2.5k
0
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1
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1.8k
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Comment: Comment: how can i solve a problem in applying a mutation on protein sequence?
2.0 years ago by barslmn ★ 2.5k
0
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1
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1.4k
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Comment: Comment: Confirming called variants
2.0 years ago by barslmn ★ 2.5k
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0
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2.6k
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Comment: Comment: NGS one-liner to call variants
2.0 years ago by barslmn ★ 2.5k
1
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1
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2.6k
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Comment: Comment: NGS one-liner to call variants
2.0 years ago by barslmn ★ 2.5k
0
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1
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2.6k
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Comment: Comment: NGS one-liner to call variants
2.0 years ago by barslmn ★ 2.5k
0
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0
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3.2k
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Comment: Comment: VEP ensemble docker and plugins
2.0 years ago by barslmn ★ 2.5k
0
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0
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2.6k
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Comment: Comment: NGS one-liner to call variants
2.0 years ago by barslmn ★ 2.5k
0
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0
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820
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Comment: Comment: Pysam pileup and Rsamtools pileup output discrepancy
2.0 years ago by barslmn ★ 2.5k
16
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9
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2.6k
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Blog: NGS one-liner to call variants
shell sequencing
updated 2.0 years ago by 45k • written 2.0 years ago by ★ 2.5k
0
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1
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3.2k
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Comment: Comment: VEP ensemble docker and plugins
2.0 years ago by barslmn ★ 2.5k
0
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1
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3.2k
views
Comment: Comment: VEP ensemble docker and plugins
updated 2.0 years ago by 45k • written 2.0 years ago by ★ 2.5k
0
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1
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3.2k
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Comment: Comment: VEP ensemble docker and plugins
2.0 years ago by barslmn ★ 2.5k
1
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0
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1.7k
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Comment: Comment: FASTQ to BAM to CRAM to FASTQ
2.0 years ago by barslmn ★ 2.5k
1
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0
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3.7k
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Comment: Comment: Want to check bam file quality
2.0 years ago by barslmn ★ 2.5k
1
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0
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1.7k
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Answer: Answer: Commands to do the following in BCFtools or recommendations for another tool
2.1 years ago by barslmn ★ 2.5k
1
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1
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893
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Comment: Comment: extract first and last n bp from fasta file from multiple fasta file in R
2.1 years ago by barslmn ★ 2.5k
0
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0
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2.5k
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Comment: Comment: Troubles launch IGV on Linux(Debian)
2.1 years ago by barslmn ★ 2.5k
0
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0
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1.0k
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Comment: Comment: Splitting VCF/BCF file into seperate gene files
2.1 years ago by barslmn ★ 2.5k
0
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1
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2.5k
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Answer: Answer: Troubles launch IGV on Linux(Debian)
2.1 years ago by barslmn ★ 2.5k
0
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1
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2.5k
views
Comment: Comment: Troubles launch IGV on Linux(Debian)
2.1 years ago by barslmn ★ 2.5k
0
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0
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1.8k
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Comment: Comment: BED files
2.1 years ago by barslmn ★ 2.5k
0
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0
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746
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Comment: Comment: Merging the filename with tsv files for master file
2.1 years ago by barslmn ★ 2.5k
0
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0
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818
views
Comment: Comment: Download an example of fully-imputed VCF files ?
2.1 years ago by barslmn ★ 2.5k
1
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1
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1.2k
views
Answer: Answer: Fetch genomic region(s) from refseq genomes
2.2 years ago by barslmn ★ 2.5k
2
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0
replies
2.3k
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Answer: Answer: What is the common practice to view WGS data on IGV?
2.2 years ago by barslmn ★ 2.5k
0
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0
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3.9k
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Comment: Comment: Converting custom VCF to standard VCF
2.2 years ago by barslmn ★ 2.5k
1
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0
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3.9k
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Answer: Answer: Converting custom VCF to standard VCF
2.2 years ago by barslmn ★ 2.5k
0
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0
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3.1k
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Comment: Comment: How to deal with duplicates between two database IDs?
2.2 years ago by barslmn ★ 2.5k
0
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1
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3.1k
views
Answer: Answer: How to deal with duplicates between two database IDs?
2.2 years ago by barslmn ★ 2.5k
0
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1
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2.7k
views
Comment: Comment: Tool to search for missing genes among genome annotation versions?
2.2 years ago by barslmn ★ 2.5k
2
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1
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2.7k
views
Answer: Answer: Tool to search for missing genes among genome annotation versions?
2.2 years ago by barslmn ★ 2.5k
1
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0
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1.1k
views
Answer: Answer: Annotate VCF with RepeatMasker
2.2 years ago by barslmn ★ 2.5k
7
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0
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997
views
Tutorial: Polygenic Risk Score Calculation
genetic-burden r prs ggplot glm
2.2 years ago by barslmn ★ 2.5k
0
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0
replies
2.2k
views
Comment: Comment: how to change the 'bcftools plugin' temp directory
2.2 years ago by barslmn ★ 2.5k
362 results • Page 2 of 8
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