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175 results • Page
4 of 4
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0
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152
views
sci-RNA-seq
cell
single
seurat
sci-rna-seq
counts
5 days ago by
kilcdincer
▴ 10
0
votes
6
replies
391
views
ComplexHeatmap - How to change fontsize of rowAnnotation
ComplexHeatmap
4 days ago by
hannes.bongartz
• 0
0
votes
2
replies
275
views
GG Sankey plot
GO
sankey_plot
gglpot
updated 4 days ago by
LauferVA
4.2k • written 5 days ago by
ijarne
• 0
0
votes
0
replies
160
views
Cell type annotation mixed with other type cells
cell
annotation.
updated 4 days ago by
GenoMax
142k • written 4 days ago by
Long
• 0
0
votes
0
replies
151
views
How can i use ESM-1v ?
VEP
ESM-1v
4 days ago by
Meto
• 0
0
votes
7
replies
4.3k
views
B allele frequency (BAF)
snp
updated 4 days ago by
aidangcruickshank
▴ 10 • written 3.7 years ago by
rthapa
▴ 90
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
4
replies
373
views
How to handle duplicated genes in TCGA data?
TCGA
GDC
mRNA
updated 4 days ago by
txema.heredia
▴ 130 • written 5 days ago by
Ngrin
• 0
0
votes
0
replies
152
views
Blog:
The Current State and Future Prospects of Long-Read Sequencing
LRS
6 days ago by
Novogene
▴ 420
0
votes
1
reply
189
views
Broad and Narrow peaks
ATAC
ChIP
seq
updated 4 days ago by
ATpoint
82k • written 4 days ago by
Jacek
▴ 20
0
votes
5
replies
325
views
calculating genomic coverage/ base overlap in R
genomics
updated 4 days ago by
1769mkc
★ 1.2k • written 7 days ago by
Xbox_27
• 0
0
votes
0
replies
148
views
Tera-scale metagenomic coassembly tool
co-assembly
Metagenomics
4 days ago by
Moinuddin
• 0
0
votes
0
replies
149
views
qPCR gene expression data analysis
qPCR
geneexpression
anova
6 days ago by
ebertomeup
• 0
0
votes
9
replies
397
views
Duplicated reads (IDs) from nanopore sequencing
bam
nanopore
sequencing
6 days ago by
njornet
▴ 20
0
votes
0
replies
139
views
Buzzled by retrieving metadata on bioprojects for an organism using "rentrez" package
R
updated 4 days ago by
Pierre Lindenbaum
162k • written 4 days ago by
Mohamed Samir
▴ 20
0
votes
2
replies
304
views
Traveler with Infernal mapping failed
r2dt
updated 3 days ago by
anton.i.petrov
• 0 • written 3 months ago by
Larissa
• 0
0
votes
1
reply
463
views
solution-Transcriptome.cpp:18:Transcriptome: exiting because of *INPUT FILE* error: could not open input file /geneInfo.tab #2142
STAR
updated 5 days ago by
GenoMax
142k • written 5 days ago by
huxiangyulove
• 0
0
votes
1
reply
31
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
0
votes
1
reply
600
views
scRNAseq quality control weird double curve in nFeature vs nCount plot
scRNA-seq
QC
single
cell
BDRhapsody
analysis
updated 6 days ago by
valdirbarth
▴ 20 • written 13 months ago by
Salomé
• 0
0
votes
4
replies
363
views
Merge clusters in Seurat UMAP
seurat
umap
5 days ago by
kilcdincer
▴ 10
0
votes
2
replies
325
views
Design for complex RNA-Seq experiment using Deseq2
Model.Matrix
RNA-Seq
Limma
DESeq2
edgeR
3 days ago by
Ezequiel
• 0
0
votes
4
replies
168
views
from CRAM to fastq
FASTQ
WGS
CRAM
updated 6 hours ago by
GenoMax
142k • written 9 hours ago by
machaalani29
• 0
0
votes
0
replies
104
views
Tool for within-sample ligand-receptor analysis (bulk RNA-seq) ?
cell-cell
communication
ligand-receptor
self-regulation
3 days ago by
DGTool
▴ 20
0
votes
0
replies
113
views
handling bio replicates for chromHMM
replicates
chromHMM
3 days ago by
Hasan_Daaboul
• 0
0
votes
8
replies
544
views
Is it Possible to "Merge" data from Replicates within a VCF SNP File
snp
vcf
genomics
plink
updated 3 days ago by
Pierre Lindenbaum
162k • written 11 days ago by
ajbarrett98
• 0
175 results • Page
4 of 4
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
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liyong
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▴ 300
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Recent Replies
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…
Comment: FastQC interpretation - 16S sequencing
by
GenoMax
142k
Since a specific region is being amplified it is expected that many of the library fragments will have identical sequences. Thus the low nu…
Comment: FastQC interpretation - 16S sequencing
by
Christopher
▴ 10
@genomax Thank you so much for replying. I was quite unsure about the qualities. One more question. There is no problem within nucleotide d…
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