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21 results • Page
1 of 1
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
9
views
Using ggplotly in R
ggplot
ggplotly
14 minutes ago by
jen
▴ 10
0
votes
1
reply
27
views
Why does assigning genes with biomart give me different values than using a transcripts_to_genes.txt file?
biomart
RNAseq
kallisto
updated 13 minutes ago by
GenoMax
142k • written 57 minutes ago by
bioinfo
▴ 150
0
votes
1
reply
50
views
Using Cutadapt to trim adapters from paired-end small RNA sequence data
trimming
adapters
cutadapt
sRNA-seq
smallRNA
updated 2 hours ago by
GenoMax
142k • written 3 hours ago by
melissa.joubert
• 0
0
votes
0
replies
35
views
Calculate allelic frequency from VEP output vcf file
VEP
variant
3 hours ago by
ramiro.barrantes
• 0
0
votes
0
replies
44
views
Is there a real ground truth for CNV data?
CNV
5 hours ago by
jennyp0706
• 0
1
vote
1
reply
78
views
sci-RNA-seq
Seurat
sci-RNA-seq
updated 1 hour ago by
Ram
43k • written 6 hours ago by
kilcdincer
▴ 10
0
votes
0
replies
40
views
Retrieving ceRNA data from the starBase or ENCORI Web API
ceRNA
ENCORI
WebAPI
microRNA
starBase
updated 6 hours ago by
GenoMax
142k • written 6 hours ago by
Bhavya
• 0
0
votes
3
replies
143
views
How to access GWAVA software of data
GWAVA
updated 6 hours ago by
GenoMax
142k • written 9 hours ago by
nonaddldy
▴ 10
0
votes
0
replies
57
views
In what situations is 'outer' typically used when using anndata.concat()?
concat
anndata
scanpy
13 hours ago by
Spring
• 0
0
votes
2
replies
124
views
Is it necessary to do genotype quality filteration after snp calling with GATK
snp
filteration
genotype
quality
GATK
10 hours ago by
IdaHao0921
• 0
0
votes
3
replies
293
views
Snakemake wrapper issue
fastqc
snakemake
updated 14 hours ago by
Wei-Chen Pan
• 0 • written 9 weeks ago by
Matvii Mykhailichenko
• 0
0
votes
0
replies
80
views
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
limma
15 hours ago by
Holly
• 0
0
votes
1
reply
121
views
How to process Bulk WES data?
WES
WGS
updated 21 hours ago by
GenoMax
142k • written 22 hours ago by
wyuan37
• 0
0
votes
1
reply
121
views
Can diamond prepdb be used to make a taxonomically aware database?
blast
diamond
taxonomy
updated 20 hours ago by
GenoMax
142k • written 23 hours ago by
cedric.blais
• 0
0
votes
1
reply
109
views
Empty .best and .sing2 Files After Running Demuxlet
Biosciences
Demuxlet
updated 21 hours ago by
Ram
43k • written 1 day ago by
eking28
• 0
0
votes
4
replies
205
views
Galaxy StringTie error
stringtie
galaxy
8 hours ago by
trkfs
• 0
1
vote
3
replies
214
views
Getting the coding_sequence.fasta from the .gff file from the AUGUSTUS gene prediction.
augustus
annotation
assembly
genome
11 hours ago by
Vijith
▴ 30
3
votes
3
replies
254
views
Gene Specific coverage from WGS data
WGS
SARS-CoV2
updated 21 hours ago by
Ram
43k • written 14 days ago by
Adyasha
• 0
0
votes
0
replies
111
views
Comparing peptide sequences with MS/MS peptide data using MaxQuant
Transcriptomics
Mass-spectrometry
Proteins
updated 21 hours ago by
Ram
43k • written 15 days ago by
atharvakarkare14
▴ 30
0
votes
0
replies
177
views
How to calculate correlation coefficient for chipseq?
chipseq
bigwigsummary
deeptools
correlation
15 hours ago by
Emily
▴ 20
0
votes
4
replies
3.6k
views
SNPEff database building error
SNP
updated 20 hours ago by
Fungal genetics
• 0 • written 7.1 years ago by
ntyagi654
• 0
21 results • Page
1 of 1
Recent Votes
A: Best de novo assembler for insect genome ?
Comment: sci-RNA-seq
The Biostar Herald for Monday, May 13, 2024
Answer: Finding variants within a subset of a BAM file
Answer: Extracting only 4-fold degenerate sites from gene sequences/alignments?
Answer: Extracting only 4-fold degenerate sites from gene sequences/alignments?
Answer: Help with IGV abbreviation
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Recent Replies
Comment: Why does assigning genes with biomart give me different values than using a tran
by
GenoMax
142k
According to HUGO there is only one [**ZSCAN2 gene**][1] and it points to the first Ensembl gene ID (ENSG00000176371). Ensembl is annotatin…
Answer: RNAseq RNA content
by
noodle
▴ 580
There are many tools for this. I recommend [gatk (picard) CollectRnaSeqMetrics][1] or alternatively [RSeQC][2] and then run [multiqc][3…
Comment: Where to get the following bed file?
by
wyuan37
• 0
Hi, I emailed them and did get the bed file! Thank you so much.
Comment: Where to get the following bed file?
by
wyuan37
• 0
Thanks! Super helpful.
Answer: Post-imputation QC for input into GWAS analyses
by
LauferVA
4.2k
1. Imputation algorithms will output log files indicating, among other things, accuracy of imputation. We can't comment on specifics as we …
Comment: Using Cutadapt to trim adapters from paired-end small RNA sequence data
by
GenoMax
142k
You can simply ignore read 2. It is not adding any information since your small RNA's are going to be small and were completely sequenced b…
Comment: Overlapping Ranges within Granges object
by
ntsopoul
▴ 60
does this work with a single .bed file?
Comment: Finding variants within a subset of a BAM file
by
ramiro.barrantes
• 0
Actually, I found a solution in downloading "bam slices" from TCGA ([https://docs.gdc.cancer.gov/API/Users_Guide/BAM_Slicing/][1]) , which …
Comment: Overlapping Ranges within Granges object
by
ntsopoul
▴ 60
![enter image description here][1]Here is some representative data and an image in igv of one gene. I have loaded the .bed file in igv. As …
Answer: RNAseq RNA content
by
ntsopoul
▴ 60
I guess he/she means raw RNA. Roughly 2% of all RNA is mRNA the rest is rRNA. I think the first thing you need to figure out is with which …
Comment: RNAseq RNA content
by
ATpoint
82k
What is "row RNA"?
Comment: Overlapping Ranges within Granges object
by
ATpoint
82k
I would probably collapse overlapping regions with `reduce` to create the second GRanges. Can you add some representative data? Using dput?
Comment: Overlapping Ranges within Granges object
by
ntsopoul
▴ 60
I have one Granges object and not two. Every IRanges entry is the critical region of the gRNA. Can this still work?
Answer: Extracting only 4-fold degenerate sites from gene sequences/alignments?
by
J.
▴ 40
FYI if you also have this problem, this seems to be a pretty good solution: https://github.com/harvardinformatics/degenotate
Comment: Biomart issue, why so few 3'utrs?
by
GenoMax
142k
AFAIK "MANE" project is only for human protein-coding genes. One potential explanation. Out of the 2000 ID's only 125 may be MANE. https:…
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