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18 results • Page
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0
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46
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Downloading full alignments from Pfam
pfam
updated 30 minutes ago by
GenoMax
141k • written 4 hours ago by
bef1
• 0
0
votes
1
reply
668
views
Can I run cellassign on samples independently if there is batch effect present?
RNA-Seq
R
cellassign
batch-effect
updated 4 hours ago by
Francesco
▴ 10 • written 3.3 years ago by
gt
▴ 30
1
vote
1
reply
162
views
ChIP-seq datasets: input samples omitted?
ChIP-seq
Normalization
NGS
updated 8 hours ago by
ATpoint
82k • written 2 days ago by
vanbelj
▴ 40
2
votes
6
replies
1.1k
views
Differential Expression using Isoseq-supplemented reference transcriptome
RNA-Seq
Salmon
Isoseq
updated 7 hours ago by
Ram
43k • written 8 months ago by
Calum
▴ 10
0
votes
0
replies
46
views
adjusting for confounders in LMER in R
confounders
LMER
R
8 hours ago by
rene.j.erhardt
▴ 20
0
votes
9
replies
220
views
How many reads for WGS Sequencing?
WGS
Bacterial-Genomics
updated 55 minutes ago by
GenoMax
141k • written 13 hours ago by
Ruqaiya
• 0
1
vote
2
replies
142
views
How to assign cell types after integration in scRNA
scRNA-seq
updated 1 hour ago by
Ram
43k • written 18 hours ago by
Francesco
▴ 10
0
votes
0
replies
74
views
STAR total splices (in Log.final) vs collapsed splice junctions (in SJ.out.tab)
STAR
18 hours ago by
tnminh89
▴ 10
8
votes
8
replies
627
views
NGS forensics: how to know if data is fabricated
fastq
STAR
NGS
Illumina
updated 3 hours ago by
Philipp Bayer
8.3k • written 20 hours ago by
noodle
▴ 530
0
votes
0
replies
80
views
Extract protein sequence
fasta
alighment
blast
20 hours ago by
anna
▴ 20
0
votes
0
replies
79
views
Filter low express genes in microarray data
microarray
20 hours ago by
Chris
▴ 260
0
votes
1
reply
265
views
absolute path for symbolic links in Snakefile
Snakemake
updated 21 hours ago by
Jesse
▴ 740 • written 8 days ago by
yifangt86
▴ 60
0
votes
2
replies
276
views
Hide positions in alignment with 99% "–" characters to ignore single sequence insertions?
alignment
gaps
updated 21 hours ago by
Jesse
▴ 740 • written 3 days ago by
Broccoli
• 0
2
votes
3
replies
260
views
Source other conda environments in a nextflow pipeline when nextflow itself is in a conda environment?
hpc
conda
nextflow
updated 22 hours ago by
Arup Ghosh
3.2k • written 1 day ago by
chaco001
▴ 40
1
vote
3
replies
277
views
Help understanding how KEGG Ortholog `K00004 ` has 3 ECs associated with it (EC:1.1.1.4, 1.1.1.-, 1.1.1.303)?
ontology
metagenomics
database
enzymes
genomics
updated 15 hours ago by
Mensur Dlakic
★ 27k • written 1 day ago by
O.rka
▴ 710
1
vote
7
replies
370
views
gvcf joint calling
WES
GATK
VCF
gVCF
7 hours ago by
zihanss
• 0
1
vote
2
replies
279
views
ScRNAseq-How to correctly choose cell type marker genes
cellAssign
cell-markers
18 hours ago by
Francesco
▴ 10
2
votes
3
replies
2.5k
views
When to use .vcf or .gvcf files from GATK HaplotypeCaller?
indel
gatk
calling
snp
variant
updated 14 hours ago by
zihanss
• 0 • written 23 months ago by
Vitor1
▴ 120
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Comment: How to assign cell types after integration in scRNA
NGS forensics: how to know if data is fabricated
Answer: ChIP-seq datasets: input samples omitted?
Comment: Help understanding how KEGG Ortholog `K00004 ` has 3 ECs associated with it (EC:
A: Deeptools plotHeatmap - Maintain Order of Input BED file
Comment: NGS forensics: how to know if data is fabricated
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Comment: Downloading full alignments from Pfam
by
GenoMax
141k
Not as convenient but the entire set of full alignments can be downloaded here: https://ftp.ebi.ac.uk/pub/databases/Pfam/current_release/Pf…
Comment: How many reads for WGS Sequencing?
by
GenoMax
141k
> What does clipped Fastq mean? Probably means that NCBI has already scanned and trimmed adapter sequencers. > both forward and revers…
Comment: How many reads for WGS Sequencing?
by
GenoMax
141k
You can use the default `adapters.fa` file included in the `resources` folder of [**BBMap suite**][1] (program to use is `bbduk.sh`) or a p…
Comment: How many reads for WGS Sequencing?
by
GenoMax
141k
Only way to find out is to try. It may work but if it is not going to then you will find that out quick (process would likely crash because…
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
Also, there is no mention of adapter sequence so which adapter sequence should i use to remove it from some other reads?
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
Also, Do you think i can reproduce at least most part of the data from the paper just on my laptop? It has 4 logical processors (Intel(R) C…
Comment: NGS forensics: how to know if data is fabricated
by
Philipp Bayer
8.3k
While I think this is an interesting case, I've before found cleaned 'raw' data on SRA. It happens: bioinformaticians receive the raw data,…
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
1. What does clipped Fastq mean? both forward and reverse reads in the same file? 2. Why would you remove 2000bp contigs? I feel it will gi…
Comment: How many reads for WGS Sequencing?
by
Ruqaiya
• 0
Well, I downloaded both the reads from-[LINK][1]. Thats all i did. Thats the only thing i need to do, right? I'l try spades. [1]: http…
Comment: How to assign cell types after integration in scRNA
by
Francesco
▴ 10
Thanks for the fast reply.. however i had only partially understood the answer. Is correct saying that low-representation integration and b…
Answer: Can I run cellassign on samples independently if there is batch effect present?
by
Francesco
▴ 10
Hi! Whenever you do make independent analysis or aggregate data and analyze them, most cell type assignment tools start from raw counts to …
Comment: gvcf joint calling
by
zihanss
• 0
Thanks for your comment, I get it now.
Answer: ChIP-seq datasets: input samples omitted?
by
ATpoint
82k
In my hands (and from what I know based on many years here) inputs are almost exclusively used during peak calling to correct for loci-spec…
Comment: How to assign cell types after integration in scRNA
by
ATpoint
82k
No difference here. After all you typically want a label per cluster/group, so either subset to the control condition to do the assignment,…
Comment: Differential Expression using Isoseq-supplemented reference transcriptome
by
gaoanwei
• 0
I found the question and ASK the GPT4 turbo
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