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0
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0
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2.0k
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Comment: C: KEGG data parse
6.4 years ago by Paul ★ 1.5k
46
votes
44
replies
24k
views
9 follow
bash loop for alignment RNA-seq data
RNA-Seq next-gen alignment
updated 19 months ago by 43k • written 10.0 years ago by ★ 1.5k
3
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0
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3.6k
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Comment: C: For loop script
6.5 years ago by Paul ★ 1.5k
1
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2
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2.0k
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Comment: C: KEGG data parse
6.5 years ago by Paul ★ 1.5k
0
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0
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3.7k
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Comment: C: Soft-clipping primer sequences in targeted sequencing: approaches and tools
6.5 years ago by Paul ★ 1.5k
0
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0
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3.7k
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Comment: C: Soft-clipping primer sequences in targeted sequencing: approaches and tools
6.5 years ago by Paul ★ 1.5k
0
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3
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3.7k
views
Answer: A: Soft-clipping primer sequences in targeted sequencing: approaches and tools
6.5 years ago by Paul ★ 1.5k
1
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1
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1.6k
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Comment: C: Data Mining from my Genomic Coordinates
6.5 years ago by Paul ★ 1.5k
9
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4
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1.6k
views
Data Mining from my Genomic Coordinates
ngs vcf database sql coordinates
updated 6.5 years ago by 87k • written 6.5 years ago by ★ 1.5k
0
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0
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1.6k
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Comment: C: Data Mining from my Genomic Coordinates
6.5 years ago by Paul ★ 1.5k
13
votes
8
replies
9.5k
views
Does Illumina Undetermined Fastq files contain barcodes
illumina demultiplexing barcodes
updated 6.5 years ago by ▴ 200 • written 8.4 years ago by ★ 1.5k
1
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0
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61k
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Answer: A: How To Sort Bed Format File
6.5 years ago by Paul ★ 1.5k
5
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1
reply
2.0k
views
Answer: A: KEGG data parse
6.5 years ago by Paul ★ 1.5k
0
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0
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2.5k
views
Comment: C: cvnkit: what is the problem here?
6.6 years ago by Paul ★ 1.5k
9
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1
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5.7k
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Answer: C: Is bcf just a bgzipped vcf?
6.6 years ago by Paul ★ 1.5k
1
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0
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12k
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Comment: C: bedtools intersect bed and vcf, coordinates problem
6.6 years ago by Paul ★ 1.5k
0
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0
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6.1k
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Comment: C: Mask or trim primer sequences in Amplicon sequencing
6.6 years ago by Paul ★ 1.5k
12
votes
10
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6.4k
views
How to extract contigs from FASTA file which contains specific sequence
fasta find extraction contig
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 1.5k
0
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0
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1.3k
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Comment: C: filter DNA sequences of defined length for certain bases at exact positions
6.7 years ago by Paul ★ 1.5k
0
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0
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1.3k
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Comment: C: filter DNA sequences of defined length for certain bases at exact positions
6.7 years ago by Paul ★ 1.5k
0
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3
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3.7k
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Comment: A: fasta files: keep only lines containing certain characters + the respective sequ
6.8 years ago by Paul ★ 1.5k
1
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0
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4.0k
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Comment: C: Downloading genomic interval for hg38
6.8 years ago by Paul ★ 1.5k
5
votes
7
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2.8k
views
merge PE reads for Transcript De-Novo Assembly ??
RNA-seq transcript assembly de-novo
updated 23 months ago by 43k • written 9.1 years ago by ★ 1.5k
1
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1
reply
2.9k
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Comment: C: SNP data filtering from VCF file
6.9 years ago by Paul ★ 1.5k
0
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0
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2.8k
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Comment: C: Compare two matrix
6.9 years ago by Paul ★ 1.5k
9
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1
reply
2.8k
views
Answer: A: Compare two matrix
6.9 years ago by Paul ★ 1.5k
0
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1
reply
2.9k
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Comment: C: SNP data filtering from VCF file
6.9 years ago by Paul ★ 1.5k
0
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2
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6.1k
views
Comment: C: Mask or trim primer sequences in Amplicon sequencing
7.0 years ago by Paul ★ 1.5k
4
votes
1
reply
4.6k
views
Answer: A: how to extract particular regions of a sequence from fasta file if its range fo
updated 7.0 years ago by 43k • written 7.3 years ago by ★ 1.5k
8
votes
0
replies
20k
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Answer: A: Best Copy Number Variation Tools
7.0 years ago by Paul ★ 1.5k
14
votes
17
replies
17k
views
7 follow
shell script for bowtie/bwa alignment pair end reads
fastq shell bwa bowtie illumina
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 1.5k
0
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0
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47k
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Comment: C: Convert Refseq Id To Gene Name
7.1 years ago by Paul ★ 1.5k
0
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0
replies
1.7k
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Comment: C: gVCF questions with "0" in the Alt field
7.1 years ago by Paul ★ 1.5k
0
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0
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1.7k
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Comment: C: gVCF questions with "0" in the Alt field
7.1 years ago by Paul ★ 1.5k
0
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0
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1.1k
views
How to interpret tandem SNP in
DNA-seq ngs varscan variants
7.1 years ago by Paul ★ 1.5k
0
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1
reply
6.1k
views
Comment: C: Mask or trim primer sequences in Amplicon sequencing
7.2 years ago by Paul ★ 1.5k
0
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1
reply
3.5k
views
Comment: C: known unmappable or poorly sequenced regions in hg38
7.2 years ago by Paul ★ 1.5k
6
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5
replies
3.5k
views
known unmappable or poorly sequenced regions in hg38
dna-seq bed ngs
updated 7.2 years ago by 13k • written 7.2 years ago by ★ 1.5k
0
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0
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3.5k
views
Comment: C: known unmappable or poorly sequenced regions in hg38
7.2 years ago by Paul ★ 1.5k
0
votes
0
replies
2.1k
views
Answer: A: converting multiple bed files to equivalent intervals
7.2 years ago by Paul ★ 1.5k
18
votes
14
replies
12k
views
7 follow
Extract specific reads from FASTQ files based on subsequence
fastq bash awk
updated 14 months ago by 43k • written 9.0 years ago by ★ 1.5k
0
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0
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4.6k
views
Comment: C: how to extract particular regions of a sequence from fasta file if its range fo
7.3 years ago by Paul ★ 1.5k
0
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0
replies
3.0k
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Comment: C: Varscan Filters Not Being Applied
7.3 years ago by Paul ★ 1.5k
0
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0
replies
4.8k
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Comment: C: 16S rRNA seq software
7.3 years ago by Paul ★ 1.5k
2
votes
0
replies
4.6k
views
Answer: A: What is the minimum coverage adequate for variant calls from Whole Genome Sequen
7.3 years ago by Paul ★ 1.5k
0
votes
2
replies
4.8k
views
Comment: A: 16S rRNA seq software
7.3 years ago by Paul ★ 1.5k
1
vote
1
reply
32k
views
Comment: C: Duplicates on Illumina
updated 7.3 years ago by 20k • written 7.3 years ago by ★ 1.5k
0
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1
reply
6.1k
views
Comment: C: Mask or trim primer sequences in Amplicon sequencing
7.3 years ago by Paul ★ 1.5k
2
votes
0
replies
3.4k
views
Answer: A: script to check the size of given contig
7.3 years ago by Paul ★ 1.5k
1
vote
0
replies
6.1k
views
Comment: C: Mask or trim primer sequences in Amplicon sequencing
7.3 years ago by Paul ★ 1.5k
165 results • Page 2 of 4
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