Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : this month
all time
today
this week
this month
this year
538 results • Page
2 of 11
Sort: Votes
Rank
Views
Votes
Replies
2
votes
6
replies
397
views
create a gene count matrix csv file from seurat object
Seurat
sparseMatrix
16 days ago by
jkim
▴ 170
2
votes
5
replies
676
views
what's the genomic location and name of gene responsible for orange and black patches in calico cats
genomes
updated 4 days ago by
Jesse
▴ 740 • written 5 days ago by
Ann
★ 2.4k
2
votes
4
replies
2.6k
views
DESeq2 inconsistent results
differential-gene-expression
RNA-Seq
DESeq2
updated 15 days ago by
Ram
43k • written 8.0 years ago by
Chris Gene
▴ 80
2
votes
2
replies
257
views
Removing adapters in all the RNAseq samples regardless if they have or not, is it correct?
fastqc
trimming
adapters
cutadapt
RNAseq
updated 21 days ago by
dsull
★ 5.8k • written 21 days ago by
ev97
▴ 20
2
votes
0
replies
1.8k
views
ComBat-seq adjustment of batch effects
RNA-Seq
ComBat-seq
SVA
edgeR
batch-effect
updated 8 days ago by
Ram
43k • written 3.4 years ago by
chatterjee.arumoy
▴ 50
2
votes
2
replies
258
views
How to row normalize a matrixplot?
scRNA-seq
RNA-seq
single-cell
scanpy
9 days ago by
bioinfo
▴ 150
2
votes
3
replies
279
views
Extracting information from my VCF file
VCF
updated 29 days ago by
bioruffo
▴ 40 • written 29 days ago by
realtreeecat
• 0
2
votes
6
replies
629
views
Overlapping and merging ChIP-seq peaks
MACS2
HOMER
ChIP-seq
peak-calling
updated 22 days ago by
Ram
43k • written 4 months ago by
zea
• 0
2
votes
5
replies
436
views
Where to find the homopolymer regions bed file for Hg002 genome?
simple-repeats
hg002
bed
homopolymer-regions
8 days ago by
Bikram Kumar
• 0
2
votes
3
replies
1.1k
views
Polishing PACBIO corrected assembly using ONT and ILLUMINA data (.fastq)
fasta
Nanopore
long-read
fastq
updated 19 days ago by
Ram
43k • written 2.8 years ago by
K
▴ 10
2
votes
7
replies
805
views
Removing duplicates
duplicates
ONT
minimap2
updated 6 days ago by
joe
▴ 510 • written 7 days ago by
quentinperriere
• 0
2
votes
2
replies
271
views
DepMap: siRNA and CRSIPR discrepancy
DepMap
updated 13 days ago by
ATpoint
82k • written 13 days ago by
Shicheng Guo
★ 9.4k
2
votes
9
replies
798
views
TCGA2STAT Error: Firehose connection
FIREHOSE
TCGA
updated 1 day ago by
LauferVA
4.2k • written 6 months ago by
Gnana
• 0
2
votes
3
replies
253
views
P-value Threshold Consideration in Multi-Sample RNA-Seq Experiment
statistics
RNA-Seq
p-value
updated 22 days ago by
Ram
43k • written 23 days ago by
Netanel
• 0
2
votes
5
replies
668
views
samtools mpileup taking too long
Bam
samtools
sam
alignment
updated 19 days ago by
Ram
43k • written 6 weeks ago by
K
• 0
2
votes
18
replies
1.6k
views
error when running phg create-maf-vcf to build a built practical haplotype graph (v2)
pangenome
phg_v2
plants
PHG
23 days ago by
b.contreras.moreira
▴ 170
2
votes
2
replies
262
views
singlecell annotation
scRNA-seq
annotation
29 days ago by
kayah
• 0
2
votes
4
replies
239
views
interpretartion of a vcf file
calling
genotype
ONT
variant
diploid
1 day ago by
samuelkalandarov2002
▴ 10
2
votes
10
replies
819
views
Only one read per run - Trying to use CellRangerv7
Fastq
CellRanger
updated 27 days ago by
Ram
43k • written 9 weeks ago by
Sky
▴ 10
2
votes
0
replies
202
views
What are good Python models/packages to predict small molecula (SMILES) binding to proteins ?
SMILES
9 days ago by
Alexander
▴ 220
1
vote
0
replies
149
views
Contradictions in GSEA results
GSEA
Enrichment-analysis
PEA
updated 27 days ago by
Ram
43k • written 27 days ago by
Tolga
▴ 30
1
vote
2
replies
269
views
Can I readmap short reads to rDNA references?
rDNA
assembly
updated 7 days ago by
Ram
43k • written 7 days ago by
aniigodwinn
• 0
1
vote
3
replies
229
views
some error in building kraken2 database
metagenome
kraken2
1 day ago by
Art1ess
• 0
1
vote
1
reply
190
views
Tool for gene function identification
Gene-Function
updated 22 days ago by
Ram
43k • written 23 days ago by
Estevão
• 0
1
vote
3
replies
190
views
Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools
bam
splicing
1 day ago by
WouterDeCoster
47k
1
vote
1
reply
459
views
PLINK multivariable GLM output: p-value without BETA and SE
linear-model
glm
plink
updated 16 days ago by
chrchang523
10k • written 16 days ago by
dsbusiness135
▴ 10
1
vote
2
replies
207
views
Flow Cytometry Data Analysis by Seurat
Seurat
updated 27 days ago by
Ram
43k • written 27 days ago by
gdfsnkfns
• 0
1
vote
0
replies
537
views
The majority of the sequences in Trinity ID do not start from start codons. Can the sequences still be used for primer design and validation?
Primers
TRINITY
5 days ago by
mathavanbioinfo
▴ 90
1
vote
2
replies
285
views
Tumour purity and ploidy estimation
Copy-number
Whole-exome-sequencing
8 days ago by
bp22
▴ 80
1
vote
1
reply
174
views
Failed to download data from EBI with ascp
EBI
aspera
updated 13 days ago by
GenoMax
141k • written 14 days ago by
biock
▴ 60
1
vote
6
replies
1.6k
views
How can Differentially Expressed Genes be found by limma package after removing batch effect by ComBat function in sva package?
limma
sva
batch-effect
R
updated 9 days ago by
Ram
43k • written 3.8 years ago by
amirmehrgou
▴ 10
1
vote
3
replies
253
views
CCA with random effects model
CCA
updated 23 days ago by
dariober
14k • written 23 days ago by
leranwangcs
▴ 120
1
vote
1
reply
175
views
Help/Direction Needed for Data Analysis of RNA
Sequencing
RNA-seq
DNA-Seq
updated 8 days ago by
dsull
★ 5.8k • written 8 days ago by
niruf
• 0
1
vote
7
replies
888
views
GATK Mutect2 Input files reference and features have incompatible contigs: No overlapping contigs found.
hg19
Mutect2
GATK
Variant-Calling
updated 29 days ago by
Ram
43k • written 9 months ago by
Manuel Sokolov Ravasqueira
▴ 100
1
vote
0
replies
155
views
DESeq2 comparing timepoints within treatment and account for background control change
RNAseq
DEG
DESeq2
updated 13 days ago by
Ram
43k • written 13 days ago by
ian.will
▴ 30
1
vote
3
replies
349
views
how to do the repeatability filtering of vcf files?
snp
vcf.
updated 23 days ago by
Pierre Lindenbaum
161k • written 24 days ago by
Max
• 0
1
vote
2
replies
921
views
vg surject for long reads
long-reads
vg
variation-graph
surject
updated 19 days ago by
Ram
43k • written 23 months ago by
ved_vyas
▴ 10
1
vote
1
reply
157
views
Failed kmer content
kmer
illumina
ngs
updated 1 day ago by
Ram
43k • written 2 days ago by
Kasturi
• 0
1
vote
2
replies
808
views
What type of normalization does removeBatchEffect function require as the input?
batch
limma
removeBatchEffect
rna-seq
batch-effect
updated 8 days ago by
Ram
43k • written 21 months ago by
ev97
▴ 20
1
vote
2
replies
1.0k
views
An issue with application of SPAdes genome assembly in Galaxy
Galaxy
SPAdes
updated 22 days ago by
Ram
43k • written 2.4 years ago by
adnan.lahuf
• 0
1
vote
2
replies
821
views
Replacing default numbers with geneNames in enhancedVolcano
EnhancedVolcano
updated 22 days ago by
Ram
43k • written 2.6 years ago by
Mohan
• 0
1
vote
3
replies
344
views
Ensembl gene id conversion
biomart
ensembl
updated 8 days ago by
ATpoint
82k • written 11 days ago by
naveedhasan2000
• 0
1
vote
2
replies
325
views
BAM to CRAM and BAM recover with smaller size
BAM
samtools
CRAM
updated 21 days ago by
jkbonfield
★ 1.2k • written 5 weeks ago by
geocarvalho
▴ 360
1
vote
0
replies
367
views
Differential expression analysis on multiple integrated datasets
microarray
Z-score
limma
differential-gene-expression
meta-analysis
updated 15 days ago by
Ram
43k • written 2.4 years ago by
michael.s
▴ 10
1
vote
3
replies
6.1k
views
Error for converting from gene symbol to Entrez IDs
Entrez-ID
org.Dr.eg.db
updated 8 days ago by
Ram
43k • written 5.5 years ago by
modarzi
▴ 170
1
vote
2
replies
625
views
Nanopore multisample variant calling
SNPs
nanopore
SNP-calling
variants
multisample
26 days ago by
colindaven
6.4k
1
vote
1
reply
222
views
Retrieve a % coverage for each transcript
RNA-seq
updated 7 days ago by
Ram
43k • written 7 days ago by
jammydodger123456
▴ 40
1
vote
4
replies
807
views
I want to calculate if the sample has whole genome duplication event or not?
sequencing
wgs
15 days ago by
Hyper_Odin
▴ 310
1
vote
1
reply
243
views
RNA seq normalization and gene gene correlation
rna-seq
pearson-correlation
vst
updated 12 days ago by
Ram
43k • written 12 days ago by
Fish
• 0
1
vote
2
replies
312
views
Extracting information from gff3 file produced by augustus
augustus
gff3
updated 9 days ago by
Istvan Albert
100k • written 11 days ago by
Jiang
• 0
538 results • Page
2 of 11
Recent Votes
Answer: Fetch table from clinvar database according to a list of rsid
Comment: Fetch table from clinvar database according to a list of rsid
Comment: Adding CB tag to bam file
Comment: alignment result
Comment: clustalo - align milions of short seq, memory issue
Answer: clustalo - align milions of short seq, memory issue
Comment: downloading genomes in fasta format from accession ids
Recent Locations •
All
Canada,
just now
France,
just now
France,
1 minute ago
Germany,
1 minute ago
Taiwan,
1 minute ago
UCLA,
2 minutes ago
China,
4 minutes ago
Recent Awards •
All
Centurion
to
analyst
▴ 30
Popular Question
to
anasjamshed
▴ 120
Popular Question
to
camillab.
▴ 160
Popular Question
to
Simone
▴ 10
Popular Question
to
carlopecoraro2
★ 2.5k
Popular Question
to
daffodil
▴ 10
Popular Question
to
Russ
▴ 500
Recent Replies
Comment: Fetch table from clinvar database according to a list of rsid
by
ashaneev07
▴ 20
so which one should i prefer? i don't need the entire results i need the condition-Germline table only. (for eg:-from, https://www.ncbi.nlm…
Comment: To get p-values for the TPM
by
dsull
★ 5.8k
OK, not sure why your intention is to use RSEM p-values for, but at least tell us the commands you ran then otherwise how are we supposed t…
Comment: Fetch table from clinvar database according to a list of rsid
by
Pierre Lindenbaum
161k
> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
Comment: different FeatureCounts output for the same data
by
sehriban.buyukkilic
▴ 10
Sure, I'll inquire about the version of Rsubread. I'll keep you posted if it works :) Thanks
Comment: different FeatureCounts output for the same data
by
sehriban.buyukkilic
▴ 10
Yeah, let me show you my featureCounts result, it looks like this. It's too low. [1]: /media/images/eb8293fe-e6ae-4b02-92e2-0ba2075b
Comment: Adding CB tag to bam file
by
Pierre Lindenbaum
161k
samtools addreplacerg is for read groups. This is not what OP asked.
Comment: Adding CB tag to bam file
by
Maria
• 0
When I try ``` samtools addreplacerg -r "@CB\tID:$cell" -o $cell.bam $LINE``` the CB tag gets add to the header, but the tag in every line …
Answer: Figures are disappeared from html report of SnpEff
by
Pierre Lindenbaum
161k
the remote website providing the javascript or/and the images is down or you're now behind a proxy. Check the firefox console: https://fire…
Comment: Fetch table from clinvar database according to a list of rsid
by
Pierre Lindenbaum
161k
ah ! and your code doesn't work because clinvar ID is not a rs-ID.
Answer: Fetch table from clinvar database according to a list of rsid
by
Pierre Lindenbaum
161k
$ cat input.rs rs11203366 rs11203367 rs874881 rs776453694 rs80324279 rs324420 rs112766203 wget -…
Comment: Highest variable features in single cell data
by
ATpoint
82k
> and these cells are not even in a single cluster. What does this mean? If you run clustering on all cells then every cell is assigned t…
Comment: Is it possible to get a list of representative genomes from a past RefSeq releas
by
Bertalan_Takacs
▴ 90
Yes, I can tell that, but as far as I see it doesn't contain any other information about the genomes, such as if they were representative i…
Answer: Hide positions in alignment with 99% "–" characters to ignore single sequence in
by
b.contreras.moreira
▴ 170
You can try <https://github.com/inab/trimal>
Comment: To get p-values for the TPM
by
VITALA
• 0
yes i want what rsem does and i did try with prior-enhanced option/pRSEM, but i think pRSEM is for chipseq data
Comment: alignment result
by
ahmad.sajad4541
• 0
Thank you so much. Should i proceed for annotation step?
Traffic: 2713 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6