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16
votes
9
replies
25k
views
7 follow
Error: unable to open file or unable to determine types for file bed file
sequencing bed bedtools
written 10.9 years ago by ▴ 240
1
vote
4
replies
3.1k
views
How to find list of genes nearest to list of intronic sequences
alignment genome sequencing
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 240
34
votes
7
replies
24k
views
6 follow
How to get all genes for a specific list of regions in R preferably using Biomart
biomart R sequencing
updated 3.3 years ago by 45k • written 10.0 years ago by ▴ 240
0
votes
1
reply
2.3k
views
How to get gene names from tophat results
RNA next-gen tophat RNA-Seq
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 240
0
votes
0
replies
2.2k
views
Seqmonk to plot feature names
seqmonk sequencing visualisation next generation
updated 10.6 years ago by 20 • written 10.7 years ago by ▴ 240
0
votes
0
replies
1.9k
views
How to get copy number change co-ordinates for all cancers from cbioportal
sequencing genome copy number
10.6 years ago by sebastianzeki0 ▴ 240
3
votes
2
replies
2.4k
views
How to find most common copy number changes in cancer
cancer sequencing copy number
updated 3.4 years ago by 45k • written 10.7 years ago by ▴ 240
1
vote
3
replies
5.0k
views
how to query biomaRt from a GRanges object
sequencing granges biomart r
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
0
votes
1
reply
5.0k
views
Comment: Comment: how to query biomaRt from a GRanges object
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
3
votes
3
replies
2.9k
views
DNA specific features affecting PCR efficiency
sequencing dna primer pcr
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
1
vote
1
reply
2.9k
views
Comment: Comment: DNA specific features affecting PCR efficiency
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
3
votes
0
replies
2.5k
views
How to find overlaps between tracks from UCSC in R
gene next-gen-sequencing r
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
0
votes
2
replies
5.2k
views
Get GC content for a list of intervals in a bed file
sequencing
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
2
votes
2
replies
2.2k
views
Bedtools trouble with double digit chromosomes
sequencing bedtools
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
1
vote
2
replies
2.9k
views
How can I query repeatmasker to give me the divergence for all the repeat families?
repeatmasker
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
0
votes
0
replies
2.9k
views
Comment: Comment: How can I query repeatmasker to give me the divergence for all the repeat famili
updated 3.6 years ago by 45k • written 10.8 years ago by ▴ 240
5
votes
2
replies
3.4k
views
Get list of LINE1 elements as a bed file
sequencing
updated 2.7 years ago by 45k • written 10.8 years ago by ▴ 240
5
votes
2
replies
25k
views
Answer: Answer: Error: unable to open file or unable to determine types for file bed file
updated 3.7 years ago by 45k • written 10.8 years ago by ▴ 240
2
votes
1
reply
2.3k
views
How to find genomic geographic commonalities between sequences
next-gen-sequencing genome Assembly
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
0
votes
0
replies
2.7k
views
How to find the most commonly affected consensus copy number range given slightly different per sample range
sequencing copy-number
updated 3.8 years ago by 45k • written 10.9 years ago by ▴ 240
8
votes
4
replies
6.1k
views
How to generate barcodes for HiSeq
HiSeq gen-sequencing next
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
1
vote
4
replies
3.1k
views
how to find chromosome position ranges common to all files
sequencing genome
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
0
votes
0
replies
3.1k
views
Comment: Comment: how to find chromosome position ranges common to all files
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
0
votes
0
replies
3.5k
views
How to label gene name only for those segments with amplifications or deletions
circos copy-number-plots
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
0
votes
0
replies
6.1k
views
Comment: Comment: How to generate barcodes for HiSeq
updated 3.7 years ago by 45k • written 10.9 years ago by ▴ 240
0
votes
0
replies
3.1k
views
Comment: A: How to find list of genes nearest to list of intronic sequences
11.0 years ago by sebastianzeki0 ▴ 240
0
votes
0
replies
3.1k
views
Comment: Comment: How to find list of genes nearest to list of intronic sequences
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 240
0
votes
1
reply
2.9k
views
Comment: A: How do I exclude low read loci from a sam file
11.0 years ago by sebastianzeki0 ▴ 240
1
vote
7
replies
2.9k
views
How do I exclude low read loci from a sam file
sequencing
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 240
0
votes
1
reply
2.9k
views
Comment: Comment: How do I exclude low read loci from a sam file
updated 3.7 years ago by 45k • written 11.0 years ago by ▴ 240
0
votes
1
reply
2.9k
views
Comment: C: How do I exclude low read loci from a sam file
11.0 years ago by sebastianzeki0 ▴ 240
31 results • Page 1 of 1
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