Traffic: 212 ip/hr
6
votes
1
answer
53
views
Variant present in 1000 genomes data but not in ESP
2
votes
2
answers
52
views
Substituting SNPs on reference genome assemblies
2
votes
1
answer
53
views
Converting GFF/GTF + reference to EMBL or GenBank ...any tools available?
3
votes
1
answer
34
views
Remove uncultured organisms from blast results with biopython
3
votes
2
answers
90
views
How to generate a heatmap of GO terms/Pathways
5
votes
3
answers
73
views
What exactly are the NCBI time limits for jobs submitted from a single IP?
2
votes
2
answers
78
views
What are the best practices for SNP identification in RNA seq transcriptome data
2
votes
1
answer
55
views
Does SAMtools tview hide PCR and optical duplicates?
1
vote
1
answer
51
views
Getting the average coverage from the coverage counts at each depth.
1
vote
3
answers
59
views
Is there is tool for variable tandem repeats finding?
0
votes
0
answers
43
views
Has the Cluster of Orthologous Genes (COGs) database been updated since 2003?
cog
1
vote
1
answer
31
views
What format are the results of a colorspace assembly using Velvet (velvetg_de) in? Double encoded or basespace?
4
votes
1
answer
60
views
Alternatives to Newbler to assemble Ion Torrent reads?
1
vote
1
answer
81
views
Is there a tutorial/guide explaining how to create a draft genome from assembled contigs?
0
votes
1
answer
31
views
Where to get the annotation file for the NimbleGen SeqCap EZ exome V1
0
votes
1
answer
47
views
Confusion related to the experiment r-th meta analysis for identifying differential gene expression
4
votes
2
answers
82
views
1 bookmark
getting sequence information from UCSC genome browser
1
vote
2
answers
100
views
2 bookmarks
ggplot2 : plotting multiple bar against same y axis. Visualization of samples!
1
vote
0
answers
82
views
1 bookmark
Multiple Sequence Alignment in C
2
votes
0
answers
56
views
Where to find chromosome band?
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