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 : all time
all time
today
this week
this month
this year
1,000 results • Page
3 of 20
Sort: replies
Rank
Views
Votes
Replies
2
votes
18
replies
1.7k
views
error when running phg create-maf-vcf to build a built practical haplotype graph (v2)
pangenome
phg_v2
plants
PHG
7 weeks ago by
b.contreras.moreira
▴ 200
5
votes
18
replies
6.8k
views
EnhancedVolcano plot error: Log2foldchange is not numeric!
R
EnhancedVolcano
4.5 years ago by
michelle.piquet
▴ 60
3
votes
18
replies
3.3k
views
Help creating Deseq2 count matrix from separate files
or
Sample
matrix
updated 2.8 years ago by
Ram
43k • written 2.9 years ago by
Nai
▴ 50
16
votes
18
replies
5.6k
views
8 follow
Python Program to read .fasta file to .txt file
Python
updated 4.7 years ago by
Mensur Dlakic
★ 27k • written 4.7 years ago by
tikshyadav19
• 0
2
votes
18
replies
2.8k
views
Bwa on multiple processor
np
mpirun
bwa
alignment
2.4 years ago by
shivangi.agarwal800
▴ 120
14
votes
18
replies
2.4k
views
Clustering in single cell
seurat
single-cell
updated 7 months ago by
e.r.zakiev
▴ 210 • written 7 months ago by
Chris
▴ 280
4
votes
18
replies
4.2k
views
Significance of reads mapping to Viruses - FusionCatcher
RNA-Seq
virus
reads
fusion
updated 21 months ago by
Ram
43k • written 8.5 years ago by
Joel TM
▴ 60
14
votes
18
replies
5.0k
views
GATK Haplotype Caller
next-gen
GATK
haplotype
caller
contigs
updated 7.4 years ago by
Biostar
20 • written 7.6 years ago by
plink_9857
▴ 50
0
votes
18
replies
1.9k
views
bcl2fastq conversion with specifying exact match of indices
genome
RNA-Seq
sequencing
updated 9 months ago by
GenoMax
142k • written 9 months ago by
Apex92
▴ 280
20
votes
17
replies
6.1k
views
HiSeq 4000 PhiX screening and removal using bbduk
spikein
filtering
bbmap
bbduk
phix
6.8 years ago by
Anand Rao
▴ 630
7
votes
17
replies
4.3k
views
Strange MA-plot using DESeq2
rna-seq
R
deseq2
updated 7.3 years ago by
Biostar
20 • written 7.5 years ago by
stan
▴ 80
16
votes
17
replies
3.2k
views
6 follow
RNA seq pipeline
RNA-Seq
6.6 years ago by
dimitrischat
▴ 210
0
votes
17
replies
3.7k
views
WGCNA error: "Error in cutreeDynamic"
rna-seq
wgcna
software error
R
next-gen
updated 2.4 years ago by
Dio
• 0 • written 5.6 years ago by
giuseppe0525
▴ 20
5
votes
17
replies
4.3k
views
Interpreting Genome_Structural_Correction Block_Bootstrap.Py
statistics
encode
10.2 years ago by
14134125465346445
★ 3.6k
3
votes
17
replies
2.9k
views
FAIRE for non-standard cultivar, mapping to reference, MAPQ
sequencing
faire
mapping
3.1 years ago by
boczniak767
▴ 850
6
votes
17
replies
2.4k
views
6 follow
Issue with reverting bam file back to fastq files
next-gen
assembly
genome
alignment
5.9 years ago by
williamsbrian5064
▴ 520
0
votes
17
replies
1.5k
views
Transcripts with no read support
RNA-Seq
alignment
assembly
salmon
3.7 years ago by
Dunois
★ 2.5k
12
votes
17
replies
4.9k
views
How do I generate all possible Newick Tree permutations for a set of species given an outgroup in Python?
Python
Newick
phylogenetics
tree
phylogeny
6.6 years ago by
anonymous1192976466
▴ 50
1
vote
17
replies
2.4k
views
Normalizing BLAST results
blast
updated 6.6 years ago by
Biostar
20 • written 6.8 years ago by
db
• 0
2
votes
17
replies
5.1k
views
Coding Potential Calculator (CPC) error
RNA-Seq
updated 6.2 years ago by
h.mon
35k • written 6.2 years ago by
Janey
▴ 30
20
votes
17
replies
3.4k
views
How to add "transcript" feature to a gtf file?
gtf
updated 10 months ago by
1769mkc
★ 1.2k • written 3.3 years ago by
pomodoro_sinensis
▴ 110
0
votes
17
replies
5.0k
views
Finding True SNPs after hard filtering on GATK
SNP
updated 20 months ago by
Ram
43k • written 8.7 years ago by
jigarnt
▴ 30
2
votes
17
replies
2.9k
views
Snakemake Megahit error
megahit
Snakemake
2.5 years ago by
blackadder
▴ 30
8
votes
17
replies
4.0k
views
Getting nan value in vcftool relatedness command?
vcftools
relatedness
6.3 years ago by
Sharon
▴ 610
2
votes
17
replies
4.4k
views
Problem With Sam To Bam Converison After Alignment Of Scaffolds To Reference
sam
bam
alignment
samtools
updated 10.4 years ago by
Devon Ryan
104k • written 10.4 years ago by
Rohit
★ 1.5k
4
votes
17
replies
2.9k
views
Cufflinks analysis and gffread
RNA-Seq
Assembly
updated 6.5 years ago by
Kevin Blighe
88k • written 6.6 years ago by
qudrat
▴ 100
9
votes
17
replies
2.2k
views
Creating intergenic bam file
R
genome
intergenic
alignment
7.8 years ago by
erincyurtman
• 0
7
votes
17
replies
6.6k
views
HeatMap: how to cluster only the rows and keep order of the heatmap's column labels as same as in the df?
R
gene
genome
5.9 years ago by
WUSCHEL
▴ 760
2
votes
17
replies
9.9k
views
7 follow
EXITING: because of fatal INPUT file error: could not open read file
mapping
genome
fastq
STAR
updated 2.2 years ago by
todd.ugine
• 0 • written 3.4 years ago by
merfer0206
• 0
0
votes
17
replies
3.1k
views
I am not able to let R read my file
R
fasta
updated 3.2 years ago by
Arup Ghosh
3.2k • written 3.2 years ago by
trejomarco6
• 0
0
votes
17
replies
2.8k
views
Fail running blastdb and blastn on my own computer
blast
6.5 years ago by
annette440
• 0
1
vote
17
replies
4.3k
views
Error executing bedops convert2bed
bedops
bed
vcf
convert2bed
7.3 years ago by
lakhujanivijay
5.8k
28
votes
17
replies
22k
views
12 follow
Dotplot for filtered pathways result
pathways
ggplot2
clusterProfiler
r
dotplot
2.5 years ago by
Leite
★ 1.3k
3
votes
17
replies
1.6k
views
copy number became inaccurate when downsampling different number fastq reads from a whole fastq file
CNV
DownSample
fastq
copy number not accurate
4.3 years ago by
lffu_0032
▴ 90
5
votes
17
replies
8.7k
views
Removing fastq duplicates
sequence
next-gen
ChIP-Seq
3.5 years ago by
C4
▴ 30
4
votes
17
replies
2.8k
views
Any strategy to find out the reason of having unusual Coefficient of Variation (CV) for gene expression data?
microarray
gene-expression
CV
error
4.9 years ago by
Jurat Shahidin
▴ 100
7
votes
17
replies
3.9k
views
How to find the differences in aligned bam files
RNA-Seq
7.2 years ago by
1769mkc
★ 1.2k
0
votes
17
replies
1.2k
views
Issues while running htseq-count
Candida-glabrata
RNA-seq
htseq-count
4 months ago by
Foad
▴ 10
1
vote
17
replies
5.8k
views
BBMap: Mapping Fails
BBTools
BBMap
Mapping
updated 8.2 years ago by
GenoMax
142k • written 8.2 years ago by
cacampbell
▴ 60
7
votes
16
replies
3.7k
views
How do I get a GFF file
snp
4.9 years ago by
apl00028
▴ 90
0
votes
16
replies
4.6k
views
Issue using MaSuRCA-3.2.6
Assembly
assembler
updated 5.7 years ago by
Biostar
20 • written 5.9 years ago by
Chvatil
▴ 130
3
votes
16
replies
1.5k
views
How to bring all reads to the same length? Any tool?
Read-length
Bed
updated 11 months ago by
Ram
43k • written 4.3 years ago by
Ankit
▴ 500
3
votes
16
replies
3.5k
views
FastTree trifurcating Root node
alignment
FastTree
Phylogenetic Tree
5.4 years ago by
Moses
▴ 150
9
votes
16
replies
1.5k
views
I am trying to select some reference genome region of a bam file, but got an error
SAMTOOLS
updated 3.8 years ago by
lieven.sterck
15k • written 3.8 years ago by
schlogl
▴ 160
2
votes
16
replies
3.1k
views
Enhancing draft genome using 10X data
10X
draft_genome
Assembly
5.8 years ago by
Mostafa
▴ 20
8
votes
16
replies
1.5k
views
what is the ideal normalistation methods for TCGA gene expression or DNA methylation dtasets?
gene
next-gen
4.4 years ago by
Chaimaa
▴ 260
9
votes
16
replies
2.0k
views
feature extraction from SNPs in R
R
gene
sequence
SNP
5.5 years ago by
bioinfo456
▴ 150
13
votes
16
replies
7.3k
views
6 follow
Confused about how to generate a consensus sequence after bwa
bwa
samtools
mpileup
5.4 years ago by
DNAngel
▴ 250
1
vote
16
replies
7.1k
views
After sorting bam file not able to index ?
alignment
next-gen
updated 5.3 years ago by
Biostar
20 • written 5.4 years ago by
sunnykevin97
▴ 980
16
votes
16
replies
3.2k
views
Using DESeq2 results for building a classifier
deseq2
RNA-Seq
differentially expressed genes
6.2 years ago by
bioinfo456
▴ 150
1,000 results • Page
3 of 20
Recent Votes
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
A: Where to find PCR duplicate reads in bam file?
A: Generate Vcf.Gz File And Its Index File Vcf.Gz.Tbi
Answer: Elbow plot question (scRNA seq data analysis - scanpy tutorial)
A: Bcftools merge taking too much time and producing large file
Answer: Kraken2 database
Recent Locations •
All
Germany,
1 minute ago
Belgium,
5 minutes ago
Oviedo,
6 minutes ago
France,
7 minutes ago
Poland,
7 minutes ago
Russia,
7 minutes ago
United Kingdom,
8 minutes ago
Recent Awards •
All
Popular Question
to
Gabriel R.
★ 2.9k
Scholar
to
diqixiaoyaoer
▴ 20
Centurion
to
marco.barr
▴ 130
Popular Question
to
Peter Chung
▴ 200
Popular Question
to
Yao
▴ 30
Popular Question
to
DareDevil
★ 4.3k
Teacher
to
Shicheng Guo
★ 9.4k
Recent Replies
Comment: What is the amount of sequencing data produced annually?
by
Mohamed
• 0
Here's a more neat version of the plot generated while writing my dissertation: ![enter image description here][1] [1]: https://raw.gi…
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
by
marco.barr
▴ 130
what a pity...
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
by
diqixiaoyaoer
▴ 20
Yes, I can. But there are only two factors that affect my data PCA distribution: groups and donor. And the rest is regarded as residual. …
Comment: ICGEB - SLIBTEC NGS Workshop: Won Best Oral Presentation Award
by
colindaven
6.4k
Please delete this as it has nothing to do with the topic of this forum, bioinformatics. Thanks
Comment: Add stats to the plot
by
marco.barr
▴ 130
if don't work try binding the stats without group. stat_data4 <- data4.ts %>% ungroup() %>% t.test(data = ., value ~ Cond…
Comment: Nextflow docker: Error response from daemon
by
Pierre Lindenbaum
161k
you should ask : https://github.com/nf-core/sarek/issues/
Comment: Where to find old version of GATK best practice
by
Pierre Lindenbaum
161k
https://github.com/gatk-workflows ?
Comment: Create a new bed file with all pairwise combinations between two other bed files
by
Alex Reynolds
35k
Hi, if you can please post a separate question with inputs and expected output, reply here with a link to it, and I'll take a look.
Comment: Create a new bed file with all pairwise combinations between two other bed files
by
J
▴ 10
Hi again Alex, sorry to ask another question about this, but how can I tweak this code to keep **all** of the SNPs that pass the threshold …
Comment: how to treat the replicates while performing WGCNA
by
mavy
▴ 10
Hello I have a quick question, I did as you said , and further added the traits, found the correlation among the modules and the traits us…
Comment: Elbow plot question (scRNA seq data analysis - scanpy tutorial)
by
ojaswinipandey
• 0
Thank you so much Dave.
Answer: Elbow plot question (scRNA seq data analysis - scanpy tutorial)
by
Dave Carlson
★ 1.7k
The y axis represents the proportion of the total variance explained by each principal component. It's negative because the value (between…
Comment: Error in using BioSampleParser tool: subscript out of bounds
by
marco.barr
▴ 130
Hi Mohamed, I also thought the same thing but we run the risk of inserting other errors perhaps by modifying the function. I tried but I ha…
Comment: Trimming tool
by
Ram
43k
Please do a few simple Google searches before asking others for help.
Comment: ICGEB - SLIBTEC NGS Workshop: Won Best Oral Presentation Award
by
Ram
43k
This post does not fit the theme of this forum.
Traffic: 2795 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