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42 results • Page
1 of 1
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Rank
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Replies
0
votes
0
replies
5
views
Error when looping over multiple columns in a data frame in R
Statistics
R
6 minutes ago by
Mohamed Samir
▴ 20
0
votes
0
replies
8
views
Phyloseq returning black bars for plot_bar
phyloseq
bioconductor
R
30 minutes ago by
Jacob
• 0
1
vote
8
replies
778
views
Random Access remote BAM files
htslib
BAM
updated 2 hours ago by
a.penatauber
• 0 • written 3 months ago by
Lucas R.F.
▴ 10
0
votes
3
replies
52
views
Mouse or Rat Gene Expression Data Similar to GTEx
whole-body
expression
atlas
updated 1 hour ago by
GenoMax
142k • written 2 hours ago by
Shicheng Guo
★ 9.4k
0
votes
0
replies
29
views
Cancer vs Normal Cell Classification Based on SNVs
cancer
3 hours ago by
dglad
• 0
0
votes
4
replies
114
views
merge overlaps and remove non overlap genomic windows
BED
intersection
overlap
2 hours ago by
reza
▴ 300
0
votes
1
reply
44
views
Flag multiple filtering steps on VCF files using VEP
FILTERING
VEP
VCF
updated 2 hours ago by
Pierre Lindenbaum
162k • written 3 hours ago by
avelarbio46
▴ 30
0
votes
1
reply
65
views
Small secondary peak for per sequence GC content - FASTQC results (bulk RNA-seq)
RNAseq
updated 4 hours ago by
GenoMax
142k • written 4 hours ago by
Fossil
• 0
1
vote
1
reply
120
views
Construction of circos plot from WGS data
WGS
Circos
updated 4 hours ago by
Ram
44k • written 12 hours ago by
Anitha
▴ 10
1
vote
3
replies
155
views
Trimmomatic running but files containing purged reads are empty
fastqc
fastq
trimmomatic
updated 6 hours ago by
GenoMax
142k • written 6 hours ago by
Wilber0x
▴ 50
0
votes
0
replies
51
views
How to find nucleotide changes and the predicted effect when comparing two genomes
BLAST
alignment
updated 4 hours ago by
Ram
44k • written 7 hours ago by
Melissa
• 0
5
votes
3
replies
145
views
FastQC interpretation - 16S sequencing
interpretation
amplicon
Fastqc
16S
updated 8 hours ago by
GenoMax
142k • written 8 hours ago by
Christopher
▴ 10
0
votes
0
replies
50
views
Subset of ATAC-seq peaks has high variance
atac-seq
edgeR
R
normalization
8 hours ago by
Tim
• 0
1
vote
5
replies
182
views
How to get the ratio of allele counts from GATK derived VCF file?
Freebayes
GATK
SNP
VCF
updated 4 hours ago by
Ram
44k • written 9 hours ago by
anikcropscience
▴ 230
0
votes
0
replies
60
views
KEGG pathway enrichment analysis in Zea mays with R
KEGG
Zea-mays
R
updated 4 hours ago by
Ram
44k • written 9 hours ago by
letizia.ottaviani
• 0
0
votes
6
replies
205
views
from CRAM to fastq
FASTQ
WGS
CRAM
updated 2 hours ago by
ATpoint
82k • written 11 hours ago by
machaalani29
• 0
0
votes
0
replies
60
views
News:
Bioinformatic Analysis of Transposable Elements course
Genome-Annotation
TE
Manual-Curation
Transposable-Elements
updated 4 hours ago by
Ram
44k • written 12 hours ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
92
views
No output when converting transcript IDs to gene symbols
RNA-seq
updated 4 hours ago by
Ram
44k • written 13 hours ago by
ashkan
▴ 160
3
votes
1
reply
123
views
vg autoindex seems stuck after a week of running
vg
pangenome
updated 14 hours ago by
Jouni Sirén
▴ 380 • written 17 hours ago by
StevieP
▴ 10
0
votes
0
replies
74
views
MAFFT alignment report
RNA
Alignment
MAFFT
Linux
updated 4 hours ago by
Ram
44k • written 14 hours ago by
Ghada
• 0
0
votes
3
replies
257
views
Kraken2 Custom Database non-deterministic results
Metagenomics
kraken2
updated 15 hours ago by
colindaven
6.4k • written 2 days ago by
Bjorn
• 0
0
votes
1
reply
118
views
How to get 2 seurat objects into a DEseq
Seurat
DEseq
updated 4 hours ago by
Ram
44k • written 22 hours ago by
He11oJe11o
• 0
0
votes
0
replies
63
views
Rescaling normalized enrichment score (NES)
heatmap
16 hours ago by
CTLong
▴ 110
0
votes
2
replies
129
views
Splitting query fasta file for Diamond Blastp make the process faster?
DIAMOND
18 hours ago by
kmat
• 0
0
votes
1
reply
118
views
Mapping difference with BWA
variant-calling
samtools
bam
BWA
genomics
updated 16 hours ago by
ATpoint
82k • written 19 hours ago by
rj.rezwan
• 0
0
votes
1
reply
123
views
How do we do quantification using stringtie merge option for all the merged samples generated.
stringtie
quantification
updated 16 hours ago by
ATpoint
82k • written 19 hours ago by
Varsha
• 0
0
votes
2
replies
130
views
samtools write-index
samtools
updated 9 hours ago by
GenoMax
142k • written 20 hours ago by
LucisTheFather
• 0
0
votes
0
replies
74
views
Kegg Pathways to Circos
Genomics
KEGG
Circos
20 hours ago by
dlera.lozano
▴ 10
0
votes
0
replies
88
views
DIFFBIND boxplot results, p value not significant
DiffBind
ChIP-seq
8 hours ago by
RD
▴ 10
3
votes
6
replies
298
views
Problem in getting geo file through GEOQUERY
geoquery
Geo
updated 4 hours ago by
Ram
44k • written 1 day ago by
anasjamshed
▴ 120
1
vote
10
replies
587
views
Add stats to the plot
R
15 hours ago by
Ghada
• 0
2
votes
4
replies
212
views
Allele count of 2 for homoplasmic MT variants in VCF
Variant-Calling
GATK
VCF
3 hours ago by
Arton
▴ 10
1
vote
3
replies
175
views
downloading chemical database from ChEMBL
ChEMBL
PyRMD
Virtual-Screening
updated 12 hours ago by
GenoMax
142k • written 1 day ago by
s
• 0
1
vote
2
replies
146
views
Multiplexing for pooled CRISPR screen sequencing
multiplex
CRISPR-screen
Illumina
5 hours ago by
Tuấn Anh
• 0
1
vote
3
replies
277
views
Functional enrichment analysis for unique gene IDs
RNA-SEQ
21 hours ago by
Pegasus
▴ 100
0
votes
3
replies
224
views
z-score of gene set
z-score
scRNA
gene-set
17 hours ago by
Hien
• 0
3
votes
2
replies
190
views
converting transcript IDs (Ensembl) to gene symbols in R
RNA-seq
updated 11 hours ago by
GenoMax
142k • written 1 day ago by
ashkan
▴ 160
0
votes
2
replies
181
views
vcf phasing
beagle
WhatsHap
phasing
17 hours ago by
safeassli
▴ 10
0
votes
4
replies
315
views
BiomartException: Query ERROR for existing dataset in BioMart
biomart
ensembl
wheat
python
pybiomart
20 hours ago by
Luqman
• 0
4
votes
11
replies
924
views
Create a new bed file with all pairwise combinations between two other bed files, based on bp distance
SNPs
BED
eqtl
bedtools
22 hours ago by
J
▴ 10
2
votes
7
replies
597
views
KEGG analysis in R
KEGG
clusterProfiler
Zea-mays
updated 12 hours ago by
letizia.ottaviani
• 0 • written 6 weeks ago by
sansan_96
▴ 90
13
votes
18
replies
6.2k
views
9 follow
Blastn, need help to increase speed
RNA-Seq
blastn
blast+
updated 15 hours ago by
Dunois
★ 2.5k • written 3.2 years ago by
chiachoong_leong93
▴ 20
42 results • Page
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Recent Votes
Answer: Microbial community analysis pipelines in metagenomics
A: What are chimeric reads?
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
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Comment: Mouse or Rat Gene Expression Data Similar to GTEx
by
GenoMax
142k
Past thread: https://www.biostars.org/p/178266/
Answer: Mouse or Rat Gene Expression Data Similar to GTEx
by
GenoMax
142k
Mouse bodymap samples : https://ncbi.nlm.nih.gov/Traces/study/?acc=PRJNA375882%20&o=acc_s%3Aa
Answer: Mouse or Rat Gene Expression Data Similar to GTEx
by
bk11
★ 2.5k
Here is the [RatGTEx][1] [1]: https://ratgtex.org
Comment: Random Access remote BAM files
by
a.penatauber
• 0
Hi Lucas, I am looking for a similar functionality as I'm working with a large volume of CRAM files on S3, and downloading them whole would…
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…
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