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
Post does not exist.
Limit : all time
all time
today
this week
this month
this year
117,084 results • Page
1 of 2342
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
11
views
Cancer vs Normal Cell Classification Based on SNVs
cancer
48 minutes ago by
dglad
• 0
0
votes
4
replies
48
views
merge overlaps and remove non overlap genomic windows
BED
intersection
overlap
just now by
reza
▴ 300
0
votes
1
reply
17
views
Flag multiple filtering steps on VCF files using VEP
FILTERING
VEP
VCF
updated 20 minutes ago by
Pierre Lindenbaum
162k • written 1 hour ago by
avelarbio46
▴ 30
0
votes
1
reply
33
views
Small secondary peak for per sequence GC content - FASTQC results (bulk RNA-seq)
RNAseq
updated 1 hour ago by
GenoMax
142k • written 1 hour ago by
Fossil
• 0
1
vote
1
reply
104
views
Construction of circos plot from WGS data
WGS
Circos
updated 2 hours ago by
Ram
44k • written 9 hours ago by
Anitha
▴ 10
799
votes
167
replies
144k
views
109 follow
News:
The Biostar Handbook. A bioinformatics e-book for beginners.
training
handbook
updated 4 months ago by
Biostar
2.8k • written 7.5 years ago by
Istvan Albert
100k
1
vote
3
replies
124
views
Trimmomatic running but files containing purged reads are empty
fastqc
fastq
trimmomatic
updated 4 hours ago by
GenoMax
142k • written 4 hours ago by
Wilber0x
▴ 50
0
votes
0
replies
44
views
How to find nucleotide changes and the predicted effect when comparing two genomes
BLAST
alignment
updated 2 hours ago by
Ram
44k • written 4 hours ago by
Melissa
• 0
5
votes
3
replies
130
views
FastQC interpretation - 16S sequencing
interpretation
amplicon
Fastqc
16S
updated 6 hours ago by
GenoMax
142k • written 6 hours ago by
Christopher
▴ 10
0
votes
0
replies
43
views
Subset of ATAC-seq peaks has high variance
atac-seq
edgeR
R
normalization
6 hours ago by
Tim
• 0
1
vote
5
replies
158
views
How to get the ratio of allele counts from GATK derived VCF file?
Freebayes
GATK
SNP
VCF
updated 2 hours ago by
Ram
44k • written 6 hours ago by
anikcropscience
▴ 230
0
votes
0
replies
52
views
KEGG pathway enrichment analysis in Zea mays with R
KEGG
Zea-mays
R
updated 2 hours ago by
Ram
44k • written 6 hours ago by
letizia.ottaviani
• 0
0
votes
6
replies
173
views
from CRAM to fastq
FASTQ
WGS
CRAM
updated just now by
ATpoint
82k • written 9 hours ago by
machaalani29
• 0
0
votes
0
replies
55
views
News:
Bioinformatic Analysis of Transposable Elements course
Genome-Annotation
TE
Manual-Curation
Transposable-Elements
updated 2 hours ago by
Ram
44k • written 9 hours ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
85
views
No output when converting transcript IDs to gene symbols
RNA-seq
updated 2 hours ago by
Ram
44k • written 10 hours ago by
ashkan
▴ 160
3
votes
1
reply
118
views
vg autoindex seems stuck after a week of running
vg
pangenome
updated 11 hours ago by
Jouni Sirén
▴ 380 • written 14 hours ago by
StevieP
▴ 10
0
votes
0
replies
69
views
MAFFT alignment report
RNA
Alignment
MAFFT
Linux
updated 2 hours ago by
Ram
44k • written 12 hours ago by
Ghada
• 0
0
votes
3
replies
252
views
Kraken2 Custom Database non-deterministic results
Metagenomics
kraken2
updated 13 hours ago by
colindaven
6.4k • written 2 days ago by
Bjorn
• 0
0
votes
1
reply
114
views
How to get 2 seurat objects into a DEseq
Seurat
DEseq
updated 2 hours ago by
Ram
44k • written 19 hours ago by
He11oJe11o
• 0
0
votes
0
replies
58
views
Rescaling normalized enrichment score (NES)
heatmap
13 hours ago by
CTLong
▴ 110
0
votes
2
replies
124
views
Splitting query fasta file for Diamond Blastp make the process faster?
DIAMOND
15 hours ago by
kmat
• 0
0
votes
1
reply
112
views
Mapping difference with BWA
variant-calling
samtools
bam
BWA
genomics
updated 13 hours ago by
ATpoint
82k • written 16 hours ago by
rj.rezwan
• 0
0
votes
1
reply
118
views
How do we do quantification using stringtie merge option for all the merged samples generated.
stringtie
quantification
updated 13 hours ago by
ATpoint
82k • written 16 hours ago by
Varsha
• 0
0
votes
2
replies
125
views
samtools write-index
samtools
updated 7 hours ago by
GenoMax
142k • written 18 hours ago by
LucisTheFather
• 0
0
votes
0
replies
71
views
Kegg Pathways to Circos
Genomics
KEGG
Circos
18 hours ago by
dlera.lozano
▴ 10
0
votes
0
replies
85
views
DIFFBIND boxplot results, p value not significant
DiffBind
ChIP-seq
5 hours ago by
RD
▴ 10
3
votes
6
replies
294
views
Problem in getting geo file through GEOQUERY
geoquery
Geo
updated 2 hours ago by
Ram
44k • written 1 day ago by
anasjamshed
▴ 120
0
votes
1
reply
149
views
Multi-ploid data in ANGSD and NGSadmix
ancestry
diploid
haploid
admixture
updated 23 hours ago by
andersdetermig
▴ 20 • written 1 day ago by
Christopher
• 0
0
votes
2
replies
229
views
transanno liftvcf "Error: length of chromosome [chr] is not equal to length in chain file. Are you using correct reference?"
liftover
transanno
23 hours ago by
ezz3
• 0
1
vote
10
replies
581
views
Add stats to the plot
R
13 hours ago by
Ghada
• 0
0
votes
4
replies
197
views
Fewer sites in vcf than in reference genome despite Emit_All_Sites argument
GATK
UnifiedGenotyper
23 hours ago by
shpak.max
▴ 50
2
votes
4
replies
177
views
Allele count of 2 for homoplasmic MT variants in VCF
Variant-Calling
GATK
VCF
31 minutes ago by
Arton
▴ 10
1
vote
3
replies
172
views
downloading chemical database from ChEMBL
ChEMBL
PyRMD
Virtual-Screening
updated 9 hours ago by
GenoMax
142k • written 1 day ago by
s
• 0
0
votes
3
replies
161
views
Where are the illumina adapters on Trimmomatic take from?
rna-seq
trimmomatic
updated 1 day ago by
GenoMax
142k • written 1 day ago by
bioinfo
▴ 150
1
vote
2
replies
133
views
Multiplexing for pooled CRISPR screen sequencing
multiplex
CRISPR-screen
Illumina
2 hours ago by
Tuấn Anh
• 0
2
votes
3
replies
1.1k
views
Is it possible to run CibersortX with a very small number of samples?
cibersortx
updated 1 day ago by
finch
• 0 • written 19 months ago by
Aspire
▴ 330
1
vote
3
replies
273
views
Functional enrichment analysis for unique gene IDs
RNA-SEQ
18 hours ago by
Pegasus
▴ 100
0
votes
2
replies
171
views
Comparing Analysis Strategies for scRNA-seq Data: Separate vs. Merged Analysis of Spleen Samples from Different Conditions
Seurat
scRNA-Seq
Single-Cell
1 day ago by
Shukai
• 0
1
vote
3
replies
175
views
Question about samtools view flags (paired reads vs. properly paired reads)
samtools
updated 1 day ago by
Pierre Lindenbaum
162k • written 1 day ago by
mrk
• 0
0
votes
3
replies
221
views
z-score of gene set
z-score
scRNA
gene-set
14 hours ago by
Hien
• 0
3
votes
2
replies
186
views
converting transcript IDs (Ensembl) to gene symbols in R
RNA-seq
updated 9 hours ago by
GenoMax
142k • written 1 day ago by
ashkan
▴ 160
0
votes
0
replies
88
views
Linking AMR Genes to Taxonomy in Soil Metagenomics
metagenomics
bacteria
wgs
AMR
resistome
updated 1 day ago by
GenoMax
142k • written 1 day ago by
LuciaNhu
• 0
1
vote
2
replies
166
views
How can we convert a vcf to fasta, so that I can blast some genes against that whole genome sequences?
blast
fasta
vcf
gene
updated 1 day ago by
Ram
44k • written 1 day ago by
Harshita
• 0
3
votes
0
replies
106
views
Comparing ATAC-seq narrowPeak Files from Chicken and Mouse
liftOver
ATAC-seq
csaw
updated 1 day ago by
Ram
44k • written 1 day ago by
Rafael Soler
★ 1.2k
0
votes
0
replies
110
views
Job:
PhD position for metagenomics analysis at the University of Udine
metagenomics
updated 1 day ago by
Ram
44k • written 1 day ago by
Fabio Marroni
★ 3.0k
3
votes
5
replies
460
views
Practical Haplotype Graph v2 not finding correct paths
Pangenome
PHG
graph
1 day ago by
beantkapoor16
▴ 10
0
votes
1
reply
128
views
DRAGEN gVCF files and joint calling GATK-GenomicsDB
DRAGEN
GenomicsDB
updated 1 day ago by
DBScan
▴ 300 • written 1 day ago by
brunomiwa
• 0
0
votes
0
replies
87
views
Last step of metagenome analysis before visualization
metagenome
python
analyis
1 day ago by
Ayda Ecem
• 0
0
votes
3
replies
157
views
Generating a Bed file from a Fasta file
bed
NullSeq
updated 1 day ago by
Ram
44k • written 1 day ago by
pirku
• 0
0
votes
3
replies
1.8k
views
Running STRUCTURE from command line
STRUCTURE
updated 1 day ago by
Ram
44k • written 3.0 years ago by
giulia.trauzzi
▴ 10
117,084 results • Page
1 of 2342
Recent Votes
Answer: Allele count of 2 for homoplasmic MT variants in VCF
Find count of reads in BAM file that fall within BED region
Up-to-date RNA-Seq Analysis Training/Courses/Papers (Dec 2017)
Up-to-date RNA-Seq Analysis Training/Courses/Papers (Dec 2017)
C: Reads mapped to another chromosome in paired-end data of RNA-seq
How to classify cells based on the expression of genes in scRNA-seq
Answer: Using GATK MarkDuplicates for targeted sequencing data
Recent Locations •
All
São Paulo,
just now
United States,
1 minute ago
Germany,
3 minutes ago
United States,
5 minutes ago
United States,
6 minutes ago
Iran,
8 minutes ago
France/Nantes/Institut du Thorax - INSERM UMR1087,
9 minutes ago
Recent Awards •
All
Scholar
to
ATpoint
82k
Popular Question
to
liyong
▴ 80
Popular Question
to
Shicheng Guo
★ 9.4k
Popular Question
to
reza
▴ 300
Popular Question
to
mhale
▴ 20
Teacher
to
Ashutosh Pandey
12k
Popular Question
to
Wilber0x
▴ 50
Recent Replies
Comment: from CRAM to fastq
by
ATpoint
82k
Yes, but I still think that with this syntax you get an uncompressed file, because samtools does not detect the gz suffix. Just take a `hea…
Comment: merge overlaps and remove non overlap genomic windows
by
reza
▴ 300
Overlap of "Ch1 200 250" and "Ch1 150 220" is "Ch1 200 220", but I want to combine windows that have overlap. Thus, my goal is to combine …
Comment: Flag multiple filtering steps on VCF files using VEP
by
Pierre Lindenbaum
162k
I don't understand that question.
Comment: merge overlaps and remove non overlap genomic windows
by
Pierre Lindenbaum
162k
> But your answer is exactly the opposite of what I want oh I see. but i don't understand the logic why: "Ch1 200 250" and "Ch1 150 220" …
Comment: merge overlaps and remove non overlap genomic windows
by
reza
▴ 300
sorry i edited my example. But your answer is exactly the opposite of what I want
Answer: merge overlaps and remove non overlap genomic windows
by
Pierre Lindenbaum
162k
> have two bed files these are not bed files. A chromosome is missing in chromosome 1 > How can I create a file from the two mention…
Comment: Small secondary peak for per sequence GC content - FASTQC results (bulk RNA-seq)
by
GenoMax
142k
Have you checked for presence of rRNA in the affected samples? That can be one possibility for these peaks. In theory if you are aligning …
Comment: Allele count of 2 for homoplasmic MT variants in VCF
by
GenoMax
142k
Please accept the answer (green check mark) to provide closure to this thread.
Comment: Trimmomatic running but files containing purged reads are empty
by
GenoMax
142k
Perhaps there were no low quality reads either.
Comment: Allele count of 2 for homoplasmic MT variants in VCF
by
Arton
▴ 10
Thank you for the helpful answer!
Comment: How to get the ratio of allele counts from GATK derived VCF file?
by
DBScan
▴ 300
I think GATK only counts informative reads in AD, do you have a DP field? DP should be closer what FreeBayes reports. You can also check GA…
Comment: Multiplexing for pooled CRISPR screen sequencing
by
Tuấn Anh
• 0
Thank you GenoMax! So would we just prepare the dual-indexed library and ask the sequencing service to do single-end sequencing?
Answer: Construction of circos plot from WGS data
by
marco.barr
▴ 130
Hi Anitha, you can take inspiration from here on which data to use and how to set up your WGS circle plot. [https://www.tandfonline.com/…
Comment: Trimmomatic running but files containing purged reads are empty
by
Wilber0x
▴ 50
Thanks for the advice, it seems like it is likely I have the incorrect adaptor sequences, though I am still surprised that no low quality r…
Answer: Trimmomatic running but files containing purged reads are empty
by
GenoMax
142k
> Why is trimmomatic not removing any reads? It is not mandatory that your data have extraneous/adapter sequence. If no extraneous sequenc…
Traffic: 2298 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