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26 results • Page
1 of 1
Sort: replies
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Views
Votes
Replies
0
votes
8
replies
212
views
Error in cnetplot enrichplot package
R
updated 13 hours ago by
Ram
43k • written 14 hours ago by
Farhad
• 0
2
votes
3
replies
119
views
interpretartion of a vcf file
calling
genotype
ONT
variant
diploid
updated 20 minutes ago by
Pierre Lindenbaum
161k • written 22 hours ago by
samuelkalandarov2002
▴ 10
1
vote
3
replies
2.4k
views
Problem to remove subset of patients with plink
plink
PED
updated 13 hours ago by
chrchang523
10k • written 6.1 years ago by
Ginevra
▴ 10
0
votes
2
replies
108
views
Should I use unpaired reads from trimmomatic
RNA-seq
QC
Trimmomatic
13 hours ago by
dxj294
• 0
0
votes
2
replies
24
views
Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools
bam
splicing
updated 12 minutes ago by
Pierre Lindenbaum
161k • written 43 minutes ago by
WouterDeCoster
47k
0
votes
2
replies
123
views
clustalo - align milions of short seq, memory issue
memory
clustalo
updated 15 hours ago by
Mensur Dlakic
★ 27k • written 21 hours ago by
emmanouil.a
▴ 120
0
votes
2
replies
147
views
Low mapping rate with Salmon
RNA-seq
Salmon
Quantification
updated 16 hours ago by
i.sudbery
19k • written 19 hours ago by
Patadu94
• 0
0
votes
1
reply
57
views
Heatmap and rna-seq
RNA-Seq
Heatmap
and
updated 1 hour ago by
Basti
★ 2.0k • written 4 hours ago by
qudrat.nii
▴ 10
0
votes
1
reply
121
views
RNA-seq bacteria contamination
RNA-seq
updated 21 hours ago by
GenoMax
141k • written 1 day ago by
sh
• 0
0
votes
1
reply
100
views
tbtool
tbtool
updated 17 hours ago by
Ram
43k • written 18 hours ago by
Raman
• 0
0
votes
1
reply
89
views
Identification of Transgene insertion sites
Transgene
Whole-Genome-Sequencing
transgene-sites
updated 14 hours ago by
Ram
43k • written 14 hours ago by
Cameron.walker9900
• 0
0
votes
1
reply
92
views
Displaced fragment length distribution in ATAC-seq
ATAC-seq
nucleosome
fragment
updated 20 hours ago by
ATpoint
81k • written 20 hours ago by
enanoide
• 0
0
votes
0
replies
8
views
Subset Seurat object from Xenium spatial data
Seurat
Xenium
Spatial
51 minutes ago by
Susmita Mandal
▴ 110
0
votes
0
replies
53
views
File with NCBI summary or Uniprot description
Refseq
function
NCBI
Uniprot
protein
24 minutes ago by
Amélie
• 0
0
votes
0
replies
62
views
Pairwise alignment and Ka/Ks computation
Pairwise-Alignment
Genomics
Ka-Ks
updated 15 hours ago by
Ram
43k • written 15 hours ago by
maxime.policarpo
▴ 200
0
votes
0
replies
65
views
How to get somatic variation based on RNA-seq data?
RNA-seq
variation
somatic
22 hours ago by
feather-W
• 0
0
votes
0
replies
64
views
Help with finding conferences in immuno-informatics/virology
virology
conferences
immunology
21 hours ago by
manaswwm
▴ 490
0
votes
0
replies
195
views
traying to make a maf from an already annotated vcf
vcf
vcf2maf
maf
maftools
VEP
20 hours ago by
Javier
• 0
0
votes
0
replies
61
views
Blasting two protein sequences vs two nucleotide sequences
gene-hunting
blast
updated 17 hours ago by
GenoMax
141k • written 17 hours ago by
Abeer
• 0
0
votes
0
replies
49
views
Analysis of the gene family of a genome.
Genome
gene-family
updated 15 hours ago by
Ram
43k • written 15 hours ago by
sansan_96
▴ 80
0
votes
0
replies
69
views
Meta analysis of two GWAS summary statistics: one study is case-control and the other is quantitative
GWAS
Meta-analysis
updated 15 hours ago by
Ram
43k • written 16 hours ago by
Oak
▴ 10
0
votes
0
replies
269
views
Choice of relatedness cutoff for GWAS of a large cohort (>100K samples)
relatedness
IBD
GWAS
updated 15 hours ago by
Ram
43k • written 14 months ago by
Oak
▴ 10
0
votes
0
replies
63
views
Annotating single cell data automatically
cell
annotation
single
23 hours ago by
Gerard
• 0
0
votes
0
replies
29
views
How do I select a GC file (gc.wig)? (How to determine the inputdata of HMMcopy)
HMMcopy
R
Copy-number-analysis
gc.wig
genome
6 hours ago by
SSSJec
• 0
0
votes
0
replies
41
views
Seurat merge and batch correction
Seurat
6 hours ago by
sooni
▴ 20
0
votes
0
replies
54
views
Filtering most similarly expressed gene (contrary to differential expression gene) with NOISeq?
NOIseq
1 hour ago by
alifafiq1
• 0
26 results • Page
1 of 1
Recent Votes
Comment: Correlation for ATAC-Seq and Chip-Seq
Answer: PDB residue serial inconsistency and PDB id&UniProt ID mismatch
Answer: PDB residue serial inconsistency and PDB id&UniProt ID mismatch
Answer: PDB residue serial inconsistency and PDB id&UniProt ID mismatch
Answer: PDB residue serial inconsistency and PDB id&UniProt ID mismatch
Comment: PDB residue serial inconsistency and PDB id&UniProt ID mismatch
Answer: What is the real meaning of relative enrichment/peak height of ChIP-seq tracks?
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Recent Replies
Comment: Filter BAM to keep only alignments at an interval, ignoring reads spliced over
by
Pierre Lindenbaum
161k
see also : https://www.biostars.org/p/9537698/ ; https://www.biostars.org/p/9464312/ ; https://www.biostars.org/p/417123/
Comment: Filter BAM to keep only alignments at an interval, ignoring reads spliced over
by
Pierre Lindenbaum
161k
what's the gray section ? it's the read you want ? do you only want the reads that end at the splice event (single point location) ?
Comment: interpretartion of a vcf file
by
Pierre Lindenbaum
161k
yes if there is more than one sample genotyped.
Comment: interpretartion of a vcf file
by
samuelkalandarov2002
▴ 10
Is it typical to observe such a profile in the context of diploid organism ?
Answer: Plots for DNA methylation data
by
Basti
★ 2.0k
Yes you can use ggplot2 to create your own plots from a table of results from a differential methylation analysis. You just need to adapt a…
Comment: Heatmap and rna-seq
by
Basti
★ 2.0k
This forum is not dedicated to this type of request, there are many online tutorials for creating heatmaps accessible with simple internet …
Answer: python file for coding potential calculator
by
atharvakarkare14
▴ 10
Download the CPC2 tool supported by python 3 from here [https://github.com/gao-lab/CPC2_standalone/releases/tag/v1.0.1][1]. Then follow …
Comment: Redirection of Duplicate PMIDs
by
LauferVA
4.2k
let me know the scope and scale of the request (e.g. I need to do this for every record in Pubmed) and can help
Comment: Redirection of Duplicate PMIDs
by
LauferVA
4.2k
how is this query itself originating?
Comment: Redirection of Duplicate PMIDs
by
dominickd
• 0
I was able to come up with a workaround using the requests library: import requests pmid = 30134295 url = 'https://pubmed.ncbi…
Comment: What is the real meaning of relative enrichment/peak height of ChIP-seq tracks?
by
HyperEvo
• 0
Thanks for you answer! Actually I have already filtered my peak according to blacklist by bedtools. You mean it's meaningless to compare on…
Answer: Redirection of Duplicate PMIDs
by
GenoMax
141k
More than likely not since the database query seems to work for the redirected PMID but not the original. $ esearch -db pubmed -query …
Comment: DYH17 Structure Prediction
by
anasjamshed
▴ 120
Blast showed PDB: 8J07_n9(human) as best template with 62.99%. I also used swissmodel to model the protein and it showed: https://swissmod…
Comment: How to slice a gvcf file with tabix?
by
Pierre Lindenbaum
161k
No, in haplotypecaller
Comment: How to slice a gvcf file with tabix?
by
Sd
• 0
Then what is the best way to do slicing for 1Mb windows? Doing `--intervals` in the GenomicsDBImport?
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