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Answer: Answer: Macbook M1 pro/M2 pro or Dell (with Ubuntu/other linux distribution) for bioinfo
updated 6 months ago by 43k • written 6 months ago by ★ 3.5k
2
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2
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4.0k
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Answer: Answer: How to parallelise a for loop in bash?
23 months ago by steve ★ 3.5k
3
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0
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2.8k
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Answer: Answer: M.S. Bioinformatics and Computational Biology: Will I be able to find a job afte
2.2 years ago by steve ★ 3.5k
0
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0
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2.7k
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Answer: Answer: Best Software for analysis of Hi-C data
2.2 years ago by steve ★ 3.5k
0
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0
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4.1k
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Answer: Answer: Filtering out samples by FORMAT attributes using bcftools
2.2 years ago by steve ★ 3.5k
0
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0
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1.7k
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Answer: Answer: How to merge variants for the same samples from different vcf files?
3.0 years ago by steve ★ 3.5k
0
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0
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91k
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Answer: Answer: Using R in Conda
3.0 years ago by steve ★ 3.5k
1
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0
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1.3k
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Answer: A: Singularity file management
3.2 years ago by steve ★ 3.5k
4
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0
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2.6k
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Answer: A: VCF AF and %Freq
3.2 years ago by steve ★ 3.5k
1
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0
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2.5k
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Answer: A: easy-to-use, fast genome browser ?
3.2 years ago by steve ★ 3.5k
4
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1
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3.8k
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Answer: A: What programming language do you use the most in your work? Which one do you lik
3.2 years ago by steve ★ 3.5k
0
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1
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1.1k
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Answer: A: Software for clinical interpretation of variants
3.3 years ago by steve ★ 3.5k
1
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1
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1.9k
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Answer: A: Is there a reasonable way to rank peaks that are common between replicates?
3.4 years ago by steve ★ 3.5k
1
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1
reply
1.5k
views
Answer: A: Merging lots of csv files in on master one
3.4 years ago by steve ★ 3.5k
0
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0
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3.1k
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Answer: A: How much RAM / how many CPUs should I allocate for Mutect2?
3.9 years ago by steve ★ 3.5k
0
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0
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2.9k
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Answer: A: Pindel installation failing due to htslib
4.2 years ago by steve ★ 3.5k
7
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1
reply
5.1k
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Answer: A: Is it possible to run IGV in batch mode without opening the GUI?
4.6 years ago by steve ★ 3.5k
3
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1
reply
4.5k
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Answer: A: Python and SLURM environment : clarifications needed
4.7 years ago by steve ★ 3.5k
0
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0
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1.8k
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Answer: A: Add tag to FORMAT tab of vcf
4.7 years ago by steve ★ 3.5k
1
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0
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7.4k
views
Answer: C: How to Demultiplex a fastq.gz file.
4.7 years ago by steve ★ 3.5k
1
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0
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1.9k
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Answer: A: How to subset fastq data based on leading nt of sequences?
4.7 years ago by steve ★ 3.5k
0
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0
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1.3k
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Answer: A: varscan2 reports wrong DP related values
4.7 years ago by steve ★ 3.5k
6
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2
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11k
views
Answer: A: Samtools problem with running (Conda)
4.8 years ago by steve ★ 3.5k
2
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1
reply
25k
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Answer: A: How read a CSV file skipping the first column using python
5.3 years ago by steve ★ 3.5k
2
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2
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17k
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Answer: C: Why I can not install anything on R?
5.5 years ago by steve ★ 3.5k
2
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0
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2.4k
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Answer: A: Create a File format to store Variant
5.8 years ago by steve ★ 3.5k
2
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1
reply
1.8k
views
Answer: A: gene name from bed file using R language of cell lines
5.9 years ago by steve ★ 3.5k
0
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1
reply
2.9k
views
Answer: A: Problems left-normalizing variants with bctools, GATK, combining with ANNOVAR an
6.0 years ago by steve ★ 3.5k
0
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1
reply
9.7k
views
Answer: C: How to get SNP identifiers from VCF file?
6.2 years ago by steve ★ 3.5k
4
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0
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2.8k
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Answer: A: Getting files from BaseMount (Using find command to loop through the symlinks)
6.2 years ago by steve ★ 3.5k
2
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0
replies
1.8k
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Answer: A: How to fetch those line having only similar characters.
6.2 years ago by steve ★ 3.5k
2
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0
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11k
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Answer: A: Can I install and run igvtools on a server?
6.3 years ago by steve ★ 3.5k
2
votes
1
reply
1.6k
views
Answer: A: How to Visulaise Genes per sample (Text visualisation)
6.3 years ago by steve ★ 3.5k
0
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1
reply
1.6k
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Answer: A: How to Visulaise Genes per sample (Text visualisation)
6.3 years ago by steve ★ 3.5k
2
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0
replies
9.3k
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Answer: A: Extract Reads In Fastq Using A Bed File.
6.4 years ago by steve ★ 3.5k
1
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0
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8.7k
views
Answer: A: Wait For A Job To Complete And Give Results Before Starting A New One
6.4 years ago by steve ★ 3.5k
3
votes
1
reply
3.6k
views
Answer: A: For loop script
6.5 years ago by steve ★ 3.5k
2
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0
replies
2.5k
views
Answer: A: Constructing server for clinical setting NextSeq
6.5 years ago by steve ★ 3.5k
5
votes
0
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7.8k
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Answer: A: Visualization of Homer mergePeaks output Venn?
6.5 years ago by steve ★ 3.5k
1
vote
0
replies
14k
views
Answer: C: Chromosome Plot In R
6.7 years ago by steve ★ 3.5k
1
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1
reply
3.5k
views
Answer: A: calling a function using glob.glob
6.8 years ago by steve ★ 3.5k
1
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0
replies
2.6k
views
Answer: A: A possible script request for a task probably cannot be done in Excel
7.2 years ago by steve ★ 3.5k
2
votes
1
reply
6.7k
views
Answer: A: How to visualize selected few ChIPseq peaks
7.5 years ago by steve ★ 3.5k
1
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0
replies
15k
views
Answer: A: How To Get The Gene Name Interactively In A R Plot
7.6 years ago by steve ★ 3.5k
1
vote
1
reply
3.9k
views
Answer: A: Sort a fasta file with ~5k sequences and match to a cluster txt file with sequen
7.6 years ago by steve ★ 3.5k
0
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0
replies
4.2k
views
Answer: A: What Is A Good Strategy For Finding Common Bacterial Sequences In A Potentially
7.7 years ago by steve ★ 3.5k
1
vote
0
replies
2.6k
views
Answer: A: Does annovar print canonical transcripts?
7.7 years ago by steve ★ 3.5k
7
votes
4
replies
13k
views
Answer: A: find positions of a short sequence in a genome
7.7 years ago by steve ★ 3.5k
1
vote
0
replies
5.1k
views
Answer: A: HOMER mergePeaks totals don't add up to peaks input
8.0 years ago by steve ★ 3.5k
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