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
315 results • Page
2 of 7
Sort: Views
Rank
Views
Votes
Replies
0
votes
5
replies
442
views
Convert gene id's to gene symbol preserving gene id's in deseq2
ensembl
r
DE
deseq2
updated 7 days ago by
Ram
40k • written 8 days ago by
dylannicoembros
• 0
3
votes
10
replies
434
views
STAR index not working
STAR
RNA-Seq
1 day ago by
camillab.
▴ 130
0
votes
1
reply
431
views
transcript id for gene id in ballgown
R
DE
ballgown
updated 29 days ago by
Ram
40k • written 20 months ago by
iamsmor
• 0
2
votes
5
replies
429
views
Dowload data from password protected cloud storage
data-transfer
wget
rclone
updated 15 days ago by
Joe
21k • written 16 days ago by
Paula
▴ 60
1
vote
0
replies
425
views
logFoldChange computed by EdgeR different from naive log2FCcomputed based on reads
edgeR
fold-change
updated 8 days ago by
Ram
40k • written 2.4 years ago by
ZheFrench
▴ 520
0
votes
0
replies
423
views
after gatk VariantAnnotator -V *_com_norm.vcf -A AlleleFraction -O *_norm_AB.vcf There "nan,nan" or "nan" in my vcf file
gatk
AlleleFraction
VariantAnnotator
updated 4 days ago by
Ram
40k • written 4 days ago by
zhuo
• 0
4
votes
4
replies
421
views
Feedback on mouse brain scRNA-seq quality control
mouse
brain
singe-cell
scRNAseq
quality-control
29 days ago by
nshenoy
▴ 50
3
votes
5
replies
419
views
Optimal number of features to use when integrate multi samples by Seurat in scRNAseq
scRNASeq
Seurat
updated 21 days ago by
Ram
40k • written 22 days ago by
alwayshope
▴ 30
1
vote
2
replies
417
views
Ranked fold changes for non-replicated data
expression
metagenomics
LogFC
fold-change
updated 8 days ago by
Ram
40k • written 18 months ago by
Tom
▴ 540
2
votes
4
replies
414
views
Help with celltype annotation
seurat
single-cell
6 days ago by
Chris
▴ 180
3
votes
4
replies
411
views
During alignment STAR has stopped at started alignment step
STAR
updated 3 days ago by
Ram
40k • written 6 weeks ago by
Santhi
• 0
3
votes
2
replies
405
views
Recommended way to normalize SmartSeq2 gene expression matrix to better match 10X expression data
rna-seq
smartseq2
r
updated 3 days ago by
yhdist
▴ 70 • written 5 days ago by
Cookin
• 0
0
votes
4
replies
402
views
PolyA and PolyG sequences in FastQC/MultiQC report
multiqc
fastqc
updated 24 days ago by
Marco Pannone
▴ 760 • written 25 days ago by
kenneditodd
▴ 20
0
votes
5
replies
395
views
How to index genome file for MethylDackel?
MethylDackel
indexing
Genome
methylation
updated 24 days ago by
ATpoint
76k • written 25 days ago by
harshraje19
▴ 40
4
votes
3
replies
378
views
Creating custom GTF file for use with Cellranger with barcode sequences
Cellranger
22 days ago by
stefano.iantorno
▴ 70
1
vote
4
replies
377
views
How to understand if a GWAS sample comes from Chromosome X or Y
python
23 days ago by
dzisis1986
▴ 60
3
votes
5
replies
377
views
Ensembl site unresponsive in clusterProfiler analyses
parallell
clusterProfiler
R
updated 16 days ago by
manaswwm
▴ 440 • written 17 days ago by
enanoide
• 0
0
votes
1
reply
376
views
Close genome comparison
Mauve
Mugsy
genome-comparison
GSAlign
updated 2 days ago by
Ram
40k • written 19 months ago by
A_heath
▴ 140
0
votes
2
replies
373
views
WES CNV analysis
CNV
WES
16 days ago by
Avinash
• 0
0
votes
3
replies
373
views
Understanding the Impact of DNA Methylation on Gene Expression in Different Genomic Regions
methylation
EPICarray
10 days ago by
Irene
• 0
0
votes
2
replies
373
views
log2fC from limma on methylation analysis
methylation
limma
minfi
fold-change
updated 8 days ago by
Ram
40k • written 11 months ago by
adeizadavid
▴ 10
2
votes
5
replies
368
views
Centrality analysis to identify TFs
TF
updated 22 days ago by
biofalconch
▴ 960 • written 24 days ago by
Chris
▴ 180
2
votes
4
replies
357
views
join the control replicates
RNA-seq
updated 8 days ago by
seidel
11k • written 9 days ago by
Jean Pierre
• 0
0
votes
0
replies
356
views
Distinction of two very close bacterial strains
mutations
bacteria
updated 2 days ago by
Ram
40k • written 2.3 years ago by
A_heath
▴ 140
0
votes
4
replies
356
views
Error using sequenza-utils with WES
WES
NGS
Sequenza
Sequenza-utils
22 days ago by
Camilo Andres
▴ 40
2
votes
5
replies
347
views
Cluster annotation in single cell
Single-cell
updated 17 days ago by
Ram
40k • written 17 days ago by
synat.keam
▴ 80
0
votes
1
reply
345
views
'syscall' is deprecated during installing jellyfish kmer counting
jellyfish
updated 15 days ago by
rubyeat88
▴ 10 • written 16 months ago by
Nur Syamilah
• 0
2
votes
2
replies
343
views
Currently lost between contigs, scaffolds and chromosomes due to positionally sorted scRNAseq bam files
bam
contigs
scRNAseq
updated 18 days ago by
ATpoint
76k • written 18 days ago by
nyxtoviopouli
• 0
0
votes
4
replies
343
views
BLAST severe RAM throttling issues on Linux (Ubuntu)
ubuntu
ram
blastx
linux
blast
updated 29 days ago by
Istvan Albert
98k • written 4 weeks ago by
Wilford203
• 0
3
votes
4
replies
342
views
Weighted analysis
RNA-seq
4 days ago by
Peter
• 0
1
vote
3
replies
340
views
What is "intersectional genetic strategy"? How does it work? What can it do?
cell-subtypes
6 days ago by
Ethan Lee
• 0
0
votes
3
replies
332
views
How to determine number of SNPs called?
Snippy
SNP
23 days ago by
SushiRoll
▴ 110
0
votes
2
replies
330
views
What is happening in the Zuker-Algorithm
R
folding
RNA
updated 21 days ago by
4galaxy77
2.8k • written 21 days ago by
Serij´s
• 0
1
vote
3
replies
329
views
SNPs that have the same position and alleles, which rsnumber to pick?
dbSNP
SNV
SNP
updated 15 days ago by
LauferVA
3.7k • written 19 days ago by
TreasureChest
• 0
0
votes
3
replies
327
views
RSubread DESeq2
RNA-seq
subread
differential-expression
deseq2
updated 5 days ago by
Ram
40k • written 14 days ago by
Beyza
• 0
0
votes
3
replies
323
views
Seeking Assistance for Interpreting a Network Representation on String-DB.org
gene-ontology
GO
enrichment
Proteome
stringdb
updated 14 days ago by
rfran010
▴ 790 • written 15 days ago by
Biomed-jeh
• 0
0
votes
5
replies
321
views
manhattan plot with vcf information
R
manhattan
vcf
updated 2 days ago by
dthorbur
▴ 550 • written 4 days ago by
sooni
▴ 10
2
votes
3
replies
320
views
How to label only a few genes of interest in heatmap of bulk RNA-seq
RNA-seq
updated 16 days ago by
Ram
40k • written 18 days ago by
Chris
▴ 180
0
votes
0
replies
320
views
GREIN tool
DEG
GREIN
updated 29 days ago by
Ram
40k • written 15 months ago by
iamsmor
• 0
1
vote
0
replies
319
views
Strand orientation and GC skew
CGView
strand-orientation
GC-skew
updated 2 days ago by
Ram
40k • written 13 months ago by
A_heath
▴ 140
0
votes
2
replies
318
views
How to load a galaxy DESeq results table into R so I can continue my workflow there
r
RNA-seq
deseq2
11 days ago by
Nicolas
• 0
5
votes
7
replies
314
views
Salmon index not progressing
salmon
updated 1 day ago by
Michael
53k • written 1 day ago by
camillab.
▴ 130
0
votes
1
reply
308
views
txt files in minfi
differential-methylation-analysis
updated 10 days ago by
Ram
40k • written 5 weeks ago by
ananta.kapoor
• 0
0
votes
2
replies
305
views
Confusion about transcript ablation
Ensembl
Variation
VEP
updated 29 days ago by
Ben_Ensembl
★ 2.3k • written 4 weeks ago by
Heiha
• 0
0
votes
3
replies
305
views
Pearson correlation with different row numbers across two datasets?
perasoncorrelation
pearson
error
updated 10 days ago by
Kevin Blighe
86k • written 11 days ago by
siefeldin
▴ 30
0
votes
2
replies
305
views
Sample size estimation with ssizeRNA in R
transcriptomics
power-analysis
RNA-seq
sample-size-estimation
17 days ago by
Nana
• 0
0
votes
3
replies
305
views
Not all variants are annotated with AF - expected or a problem?
Alignment
WGS
Calling
Variant
updated 15 days ago by
GenoMax
134k • written 15 days ago by
Luiz
▴ 30
3
votes
4
replies
301
views
Visualization of multiple sequence alignment quality
blastp
blast
msa
updated 18 days ago by
GenoMax
134k • written 18 days ago by
dec986
▴ 370
0
votes
3
replies
298
views
Calculating MAF from EAF from a GWAS summary statistics file in R
R
EAF
updated 16 days ago by
Ram
40k • written 18 days ago by
namraahmad173
• 0
1
vote
4
replies
297
views
htseq-count reports count values for deleted genes
rna-seq
htseq
11 days ago by
kmyers2
▴ 80
315 results • Page
2 of 7
Recent Votes
Answer: Ties in reranked list
Answer: Ties in reranked list
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
Comment: Error in bowtie2
Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
Comment: Using STAR aligner to build index of hg38
Answer: How to sort using samtools
Recent Locations •
All
San Francisco,
7 minutes ago
Netherlands,
19 minutes ago
ETH Zurich,
22 minutes ago
Sweden,
27 minutes ago
Canada,
40 minutes ago
Denmark,
41 minutes ago
Cambridge, MA,
44 minutes ago
Recent Awards •
All
Popular Question
to
langziv
▴ 50
Popular Question
to
Emily
▴ 30
Popular Question
to
Bogdan
★ 1.4k
Popular Question
to
paria
▴ 70
Popular Question
to
Ahmed.waraky
▴ 10
Teacher
to
fracarb8
★ 1.2k
Scholar
to
antonioggsousa
2.8k
Recent Replies
Comment: Ties in reranked list
by
Hamza
• 0
I had actually accidentally used ranks instead of Entrez gene ids (but switched later to human Ensembl gene ids). However, without your com…
Comment: Hugo_Symbol to Entrez ID
by
shakyaram079
• 0
Yes sure. These are all gene IDs BZRAP1, C19orf60, TCEB3 and so on.
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I tried the commands you recommended in the bash/command line. When I tried `find "${bam_directory}" -type f -name "*.bam" | xargs samtools…
Comment: Hugo_Symbol to Entrez ID
by
GenoMax
134k
Can you provide some examples of HUGO ID's you are unable to convert?
Comment: Using STAR aligner to build index of hg38
by
GenoMax
134k
GTF file includes gene models/annotation information. You could also use a program like `salmon/kallisto` with just human transcriptome to…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
then test each files. find "${bam_directory}" -type f -name "*.bam" | xargs samtools quickcheck file "${reference_gen…
Answer: Ties in reranked list
by
alserg
▴ 860
The problem here is not the ties, but that your gene IDs in the pathway list (ensemble human genes) does not match the names of the stats v…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I did not use the space between the `-u` flag and the `-o` flag (the blank line) but I did do what you recommended: # Run CuffDiff wit…
Answer: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
how about simply trying: ``` cuffdiff -u "${annotation_gtf}" \ -o "${output_directory}" \ -b "${reference_genome}" \ -p "${num_th…
Comment: Using STAR aligner to build index of hg38
by
Grace
• 0
Yes, I know also need a GTF file. So the GTF file will include RNA information? Thanks for your answer!!
Comment: STAR Intron Motif Script Gives Segmentation fault Error
by
Y
• 0
I will try and figure it out on my own given what you all have mentioned. Thank you for your time.
Comment: Using STAR aligner to build index of hg38
by
Amitm
★ 2.2k
Have you gone through the manual [here][1]. In addition to the genome fasta file, you would also need a GTF file (of gene annotations) to b…
Comment: Highly inflated p-values in GWAS by regenie
by
4galaxy77
2.8k
You still definitely need to include principle components as covariates, even if your data is from the same ethnicity. Not including those …
Answer: How to create structural variants ground truth for alignment of two long-read ge
by
Christophe
• 0
Hi, D-genies is using minimap2 to align both genomes and minimap2 is chaining local alignments to produce a global one. If the SV are sm…
Comment: Ties in reranked list
by
Hamza
• 0
In this case there are no results in my fgsea object unfortunately
Traffic: 2109 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