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: Views
Rank
Views
Votes
Replies
40
votes
7
replies
63k
views
Clustering Data (Rna-Seq) Using R To Produce A Heatmap
r
rna
heatmap
clustering
gene
updated 15 months ago by
Ram
40k • written 11.9 years ago by
Kanne
▴ 450
25
votes
5
replies
61k
views
7 follow
Rpkm Calculation For Genes
rpkm
rna-seq
updated 11.0 years ago by
JC
13k • written 11.0 years ago by
siddharth.sethi5
▴ 270
36
votes
14
replies
61k
views
9 follow
What Is The Difference Between Hg18 And Hg19?
genome
hg
hg
updated 11.7 years ago by
Jorge Amigo
14k • written 11.7 years ago by
Sara
▴ 170
156
votes
24
replies
60k
views
19 follow
Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
alternative-splicing
splicing
rna-seq
updated 3 months ago by
Ram
40k • written 10.6 years ago by
Nicolas Rosewick
10k
328
votes
54
replies
60k
views
45 follow
What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
genome
visualization
updated 12 months ago by
Kevin Blighe
86k • written 13.5 years ago by
brentp
24k
62
votes
22
replies
60k
views
16 follow
How To Convert Gencode Gtf Into Bed Format ?
gtf
bed
updated 9 months ago by
leshaker
• 0 • written 10.9 years ago by
biorepine
★ 1.5k
102
votes
30
replies
60k
views
25 follow
Tools To Find Gene Ontology Term Enrichment
gene
enrichment
updated 3 months ago by
Ram
40k • written 13.6 years ago by
Biostar User
★ 1.0k
149
votes
35
replies
60k
views
33 follow
Tutorial:
Tools For Metagenomic Data Analysis
metagenomics
next-gen
updated 7 months ago by
Ram
40k • written 10.8 years ago by
vijay
★ 1.6k
91
votes
25
replies
60k
views
18 follow
Best Practices/Softwares To Calculate Ka/Ks Ratio
kaks
selection
software
updated 13 months ago by
Michael
53k • written 12.6 years ago by
Jarretinha
3.4k
135
votes
33
replies
60k
views
19 follow
VCF files: Change Chromosome Notation
vcf
next-gen
sequence
updated 11 months ago by
Ram
40k • written 9.4 years ago by
Quak
▴ 480
27
votes
21
replies
59k
views
21 follow
Public Electronic Health Records Database
database
updated 2.0 years ago by
Ram
40k • written 10.4 years ago by
Abhi
★ 1.6k
53
votes
20
replies
59k
views
14 follow
Bam Header Edit
bam
updated 13 months ago by
Ram
40k • written 11.3 years ago by
Ashutosh Pandey
12k
53
votes
8
replies
59k
views
8 follow
What Is A Good Threshold For Log2 Fold Change?
microarray
gene
updated 8.6 years ago by
Biostar
20 • written 12.6 years ago by
Some
▴ 90
100
votes
6
replies
59k
views
6 follow
Insert Size And Fragment Size ?
23 months ago by
Nicolas Rosewick
10k
39
votes
20
replies
59k
views
8 follow
How to convert to .SRA files to .FQ (FASTQ)
fastq
FASTQ
sra
RNA-Seq
SRAA
updated 19 months ago by
aimanbarki
▴ 20 • written 9.1 years ago by
Veli Kaan Aydin
▴ 50
2
votes
10
replies
59k
views
R: remove rows by a list of rownames
R
updated 17 months ago by
Ram
40k • written 8.7 years ago by
silvi_free88
▴ 50
17
votes
6
replies
59k
views
Turn Off Blast Search On Reverse Complement Strand In Blastn
sequence
blast
updated 3.1 years ago by
yasopi9568
• 0 • written 13.6 years ago by
Zhaorong
★ 1.4k
90
votes
44
replies
59k
views
28 follow
Tool to generate proportional Venn Diagrams?
visualization
updated 17 months ago by
Ram
40k • written 12.5 years ago by
Ryan D
★ 3.4k
37
votes
5
replies
58k
views
Idenity, e value or bitscore ?
blast
annotation
updated 4.3 years ago by
alslonik
▴ 300 • written 7.5 years ago by
Leo
▴ 60
1
vote
3
replies
58k
views
Error in loading R package "GO.db" in installing WGCNA R package
R
updated 16 months ago by
Ram
40k • written 8.6 years ago by
zaynabmousavian
▴ 10
1
vote
6
replies
58k
views
Error in read.table(file = file, header = header, sep = sep, quote = quote, : duplicate 'row.names' are not allowed
R
updated 6 months ago by
Ram
40k • written 6.8 years ago by
IOM
• 0
19
votes
2
replies
57k
views
Keeping pheatmap colour range the same for different data sets
R
RNA-Seq
pheatmap
updated 7.4 years ago by
Selenocysteine
▴ 620 • written 7.4 years ago by
as9309
▴ 60
93
votes
19
replies
57k
views
18 follow
What Is A Good Phylogenetic Tree Display Program For Large Data Sets?
phylogenetics-tree
updated 3 months ago by
Ram
40k • written 13.1 years ago by
Niek De Klein
★ 2.6k
164
votes
70
replies
57k
views
34 follow
How To Efficiently Parse A Huge Fastq File?
next-gen
sequencing
fastq
parsing
updated 11.7 years ago by
Ric
▴ 430 • written 12.2 years ago by
Panos
★ 1.8k
7
votes
3
replies
57k
views
what is the difference between single end and paired end in sequencing
RNA-Seq
updated 23 months ago by
Ram
40k • written 9.3 years ago by
M K
▴ 620
76
votes
24
replies
57k
views
16 follow
How To Sort Bed Format File
bed
updated 11 months ago by
Pierre Lindenbaum
157k • written 10.6 years ago by
lyz10302012
▴ 450
131
votes
22
replies
57k
views
15 follow
How do I explain the difference between edgeR, LIMMA, DESeq etc. to experimental Biologist/non-bioinformatician
gene
LIMMA
edgeR
updated 3 months ago by
Kevin Blighe
86k • written 5.9 years ago by
Mike
★ 1.9k
85
votes
2
replies
56k
views
6 follow
Tutorial:
How To Ask Good Questions On Technical And Scientific Forums
how-to
updated 7 months ago by
Ram
40k • written 10.3 years ago by
Eric Normandeau
11k
15
votes
5
replies
55k
views
R Help: For Loop Over Range Of Number And Calculate Average Using An If Statement
r
updated 7.7 years ago by
Biostar
20 • written 9.7 years ago by
714
▴ 110
62
votes
24
replies
55k
views
20 follow
Download All The Bacterial Genomes From Ncbi
ncbi
updated 20 months ago by
Ram
40k • written 10.7 years ago by
rehma.ar
▴ 290
50
votes
5
replies
55k
views
6 follow
Subsampling Bam File With Samtools
samtools
bam
updated 2.0 years ago by
eidriangm
▴ 50 • written 10.2 years ago by
madbessoul
▴ 250
12
votes
13
replies
55k
views
pheatmap: Error in hclust(d, method = method) : NA/NaN/Inf in foreign function call (arg 10)
R
RNA-Seq
pheatmap
arg10
updated 2.7 years ago by
henry-keen
▴ 40 • written 3.3 years ago by
camillab.
▴ 140
12
votes
7
replies
55k
views
Use Python To List Filename With Specific Extensions.
python
updated 12.3 years ago by
Giovanni M Dall'Olio
28k • written 12.3 years ago by
Bioscientist
★ 1.7k
72
votes
18
replies
54k
views
13 follow
Extracting Multiple Fasta Sequences At A Time From A File Containing Many Sequences
fasta
sequence
parsing
perl
updated 13.0 years ago by
Peter
6.0k • written 13.0 years ago by
Sarah
▴ 110
38
votes
41
replies
54k
views
9 follow
Volcano Plot from DEseq2
R
written 5.9 years ago by
1769mkc
★ 1.1k
30
votes
8
replies
54k
views
7 follow
R: How to convert log2FC (Fold Change) obtained by limma's topTable() function to FC
limma
microarray
topTable
R
updated 14 months ago by
Ram
40k • written 9.4 years ago by
komal.rathi
★ 4.1k
47
votes
10
replies
54k
views
7 follow
RNA-seq: Explain STAR quantMode geneCounts values
RNA-Seq
STAR
Differential expression
updated 5.5 years ago by
Tao
▴ 520 • written 6.9 years ago by
williantafsilva
▴ 360
0
votes
6
replies
54k
views
Error in dimnames(x) <- dn : length of 'dimnames' [1] not equal to array extent
R
heatmap
error
updated 2.4 years ago by
Abdul Aziz
• 0 • written 4.6 years ago by
luzglongoria
▴ 50
28
votes
22
replies
54k
views
11 follow
How To Convert List Of Entrez Ids Into Gene Name
r
genomics
entrez
updated 3 months ago by
cwang3444
• 0 • written 10.4 years ago by
grosy
▴ 90
61
votes
12
replies
53k
views
7 follow
Recommended cutoff for FDR - 0.05 or 0.1
RNA-Seq
R
updated 2.5 years ago by
George
• 0 • written 7.1 years ago by
aggregatibacter
▴ 180
84
votes
12
replies
53k
views
9 follow
What are chimeric reads?
sequence
updated 20 months ago by
Ram
40k • written 9.0 years ago by
zhangz.cs
▴ 290
42
votes
26
replies
53k
views
11 follow
How To Interpret A T-Test Output Produced By R
statistics
updated 10.2 years ago by
Biostar
20 • written 11.2 years ago by
Panos
★ 1.8k
77
votes
27
replies
53k
views
20 follow
How To Write Data In A Granges Object To A Bed File.
bed
updated 13 months ago by
Johan Zicola
▴ 70 • written 9.8 years ago by
Ram
▴ 180
16
votes
30
replies
53k
views
9 follow
Retrieve The Fasta Nucleic Sequences Of A List Of Ncbi Accession Number Of Proteins
dna
sequence
retrieval
perl
bioperl
updated 12.6 years ago by
Palu
▴ 290 • written 12.6 years ago by
Samad
▴ 90
57
votes
22
replies
53k
views
14 follow
How Can I Know The Length Of Mapped Reads From Bam File?
bam
mapping
updated 14 months ago by
Alex Reynolds
35k • written 10.6 years ago by
Jordan
★ 1.3k
146
votes
34
replies
53k
views
17 follow
Tutorial:
Working with MAF files (Mutation Annotation Format) from the TCGA (The Cancer Genome Atlas)
music
cancer
tcga
mutation
maf
updated 7 months ago by
Ram
40k • written 10.5 years ago by
Cyriac Kandoth
6.0k
95
votes
5
replies
53k
views
Difference between Hard Clip and Soft Clip in Samtools CIGAR string
samtools
clipped-reads
soft-clip
bam
hard-clip
updated 21 months ago by
Ram
40k • written 9.1 years ago by
QVINTVS_FABIVS_MAXIMVS
★ 2.5k
1.2k
votes
206
replies
53k
views
108 follow
Forum:
What Are The Most Common Stupid Mistakes In Bioinformatics?
software
updated 4 months ago by
Raony Guimarães
★ 1.2k • written 12.5 years ago by
Jeremy Leipzig
21k
10
votes
8
replies
52k
views
geom_bar plot with several variables
R
ggplot2
updated 4.2 years ago by
gpushpaganesan
• 0 • written 4.7 years ago by
jordi.planells
▴ 450
80
votes
27
replies
52k
views
23 follow
Renaming Entries In A Fasta File
fasta
updated 7.4 years ago by
noirot.celine
▴ 50 • written 11.0 years ago by
thiago84naka
▴ 130
1,000 results • Page
3 of 20
Recent Votes
A: .gstmp extension on .bam files downloaded from google bucket; and EOF marker is
Comment: Significance testing of top vs. random SNPs
Answer: Search RCSB with a list of protein names?
A: running RAxML and MrBayes over concatinated multiple sequence alignments
Comment: Weirdness in annotation (missing allele frequencies)
Comment: Weirdness in annotation (missing allele frequencies)
Comment: ncbi error report log for validate fastq issue
Recent Locations •
All
Japan,
3 minutes ago
United States,
9 minutes ago
United States,
17 minutes ago
Seattle, WA USA,
23 minutes ago
Pakistan,
25 minutes ago
China,
28 minutes ago
India,
38 minutes ago
Recent Awards •
All
Commentator
to
dsull
★ 4.8k
Scholar
to
liorglic
★ 1.3k
Popular Question
to
natasha.sernova
★ 3.9k
Popular Question
to
ntsopoul
▴ 50
Teacher
to
benformatics
3.8k
Popular Question
to
iislam
• 0
Scholar
to
ATpoint
77k
Recent Replies
Comment: Getting the overlap between two GTF files
by
Alex Reynolds
35k
What would that be?
Answer: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
@ialbert ,I am deeply immersed in the fog and request the help ,please
Comment: bedtools intersect by position & stand not working even with common regions
by
rfran010
▴ 830
are you sure bedtools can handle the non-standard location of strand information?
Answer: Getting the overlap between two GTF files
by
rfran010
▴ 830
Maybe somebody knows something I don't, but I feel like bedtools should be able to handle your gtf files directly. If it's not done alre…
Answer: vcf.gz to vcf
by
Mark
★ 1.3k
As the error says, the file is not compressed. In linux the file extension is essentially optional. The file could be named `my.vcf.txt` ye…
Answer: Search RCSB with a list of protein names?
by
Jiyao Wang
▴ 340
You can use NCBI esearch to search the protein names against the structure database to get the PDB IDs, then retrieve the structures.
Answer: How to get ncol = nrow?
by
Mark
★ 1.3k
Without your actual data, it's hard to assist. I think what you're asking is 'how do I rename the rows of my dataframe(s)'. Taking the …
Comment: MAKER: WARNING: Could not get initialization lock. Trying Again...
by
GenoMax
134k
What kind of hardware are you running this on? You need to have the right kind of hardware (multiple CPU's not just cores), MPI libraries a…
Answer: Getting the overlap between two GTF files
by
Alex Reynolds
35k
Using `bedops --intersect` and `gtf2bed` will get their common genomic space: ``` bedops --intersect <(gtf2bed < transcripts.gtf) <(gtf2be…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
```bash # Obtain the makefile curl -s http://data.biostarhandbook.com/make/snpcall.mk > Makefile # Run the makefile make vcf ``` Error me…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
> System Information: Ubuntu 22.04 (WSL2) > > Shell: zsh > > Installation Verification: Yes, doctor.py OK [1]: https://www.biostarhand…
Comment: Retrieve The Reads And Fastq From Bam File
by
Reem
• 0
Did it affect the bamtofastq output file? if so how did you solve the problem? Thanks
Answer: How to import bigwig files into igvR
by
Trivas
★ 1.5k
You could try seeing if this fixes your issue with rtracklayer: https://support.bioconductor.org/p/p133244/
Comment: Weirdness in annotation (missing allele frequencies)
by
Jeremy Leipzig
21k
0.60625 is 97/160 so if you have 80 individuals in your VCF that's an internal allele frequency, not gnomAD
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Yes, I was confused as well. I think the same. Maybe Annovar uses some other resources besides gnomad, but it does not make sense. Also, I …
Traffic: 1283 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