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comments
0
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0
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267
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Comment:
Comment: Can I compare kallisto counts from samples with different amount of reads?
9 days ago by
bioinfo
▴ 150
0
votes
0
replies
259
views
Comment:
Comment: How to row normalize a matrixplot?
10 days ago by
bioinfo
▴ 150
1
vote
2
replies
267
views
Can I compare kallisto counts from samples with different amount of reads?
RNA-seq
kallisto
9 days ago by
bioinfo
▴ 150
0
votes
0
replies
153
views
How should I make kallisto indexes?
kallisto
updated 10 days ago by
GenoMax
141k • written 10 days ago by
bioinfo
▴ 150
2
votes
2
replies
259
views
How to row normalize a matrixplot?
scRNA-seq
RNA-seq
single-cell
scanpy
10 days ago by
bioinfo
▴ 150
0
votes
1
reply
198
views
How to do DE between cells expressing specific gene in scanpy?
scRNA-seq
single-cell
scanpy
updated 21 days ago by
Ram
43k • written 21 days ago by
bioinfo
▴ 150
0
votes
0
replies
289
views
Comment:
Comment: How to compare bulk RNA seq data demultiplexed in different ways?
24 days ago by
bioinfo
▴ 150
0
votes
1
reply
289
views
Comment:
Comment: How to compare bulk RNA seq data demultiplexed in different ways?
24 days ago by
bioinfo
▴ 150
0
votes
5
replies
289
views
How to compare bulk RNA seq data demultiplexed in different ways?
RNA-seq
updated 21 days ago by
Ram
43k • written 24 days ago by
bioinfo
▴ 150
0
votes
1
reply
483
views
Comment:
Comment: How does kallisto handle multi mapped reads?
9 weeks ago by
bioinfo
▴ 150
0
votes
1
reply
483
views
Comment:
Comment: How does kallisto handle multi mapped reads?
9 weeks ago by
bioinfo
▴ 150
3
votes
7
replies
483
views
How does kallisto handle multi mapped reads?
kallisto
updated 9 weeks ago by
dsull
★ 5.8k • written 9 weeks ago by
bioinfo
▴ 150
0
votes
2
replies
341
views
How to add motifs in cellranger-arc reference?
gtf
scRNAseq
fasta
cellranger
updated 7 days ago by
Ehsan
• 0 • written 9 weeks ago by
bioinfo
▴ 150
0
votes
0
replies
281
views
How to do KEGG pathway analysis when I have a gene with multiple entrez IDs?
biomart
kegg
deseq2
4 months ago by
bioinfo
▴ 150
4
votes
2
replies
609
views
Does DESeq2 correct for library size when importing the counts with DESeqDataSetFromMatrix?
rna-seq
deseq2
updated 5 months ago by
i.sudbery
19k • written 5 months ago by
bioinfo
▴ 150
0
votes
1
reply
961
views
Comment:
Comment: How much adapters is it ok to keep in my samples after RNA seq?
5 months ago by
bioinfo
▴ 150
0
votes
1
reply
961
views
Comment:
Comment: How much adapters is it ok to keep in my samples after RNA seq?
5 months ago by
bioinfo
▴ 150
0
votes
1
reply
961
views
Comment:
Comment: How much adapters is it ok to keep in my samples after RNA seq?
5 months ago by
bioinfo
▴ 150
3
votes
7
replies
961
views
How much adapters is it ok to keep in my samples after RNA seq?
RNA-seq
illumina
adapters
updated 21 days ago by
Ram
43k • written 5 months ago by
bioinfo
▴ 150
0
votes
0
replies
667
views
Comment:
Comment: Why am I getting different results with kallisto?
5 months ago by
bioinfo
▴ 150
0
votes
1
reply
667
views
Comment:
Comment: Why am I getting different results with kallisto?
5 months ago by
bioinfo
▴ 150
0
votes
1
reply
667
views
Comment:
Comment: Why am I getting different results with kallisto?
5 months ago by
bioinfo
▴ 150
3
votes
4
replies
667
views
Why am I getting different results with kallisto?
kallisto
5 months ago by
bioinfo
▴ 150
0
votes
1
reply
469
views
Comment:
Comment: Are truseq adapter sequences picked up by FASTQC?
5 months ago by
bioinfo
▴ 150
2
votes
3
replies
469
views
Are truseq adapter sequences picked up by FASTQC?
fastqc
truseq
updated 5 months ago by
GenoMax
141k • written 5 months ago by
bioinfo
▴ 150
0
votes
0
replies
326
views
How to convert dataframe properly to anndata?
single-cell
python
anndata
updated 21 days ago by
Ram
43k • written 6 months ago by
bioinfo
▴ 150
0
votes
0
replies
324
views
How to import filtered_tf_bc_matrix and add it to my anndata object?
python
anndata
atac-seq
updated 21 days ago by
Ram
43k • written 6 months ago by
bioinfo
▴ 150
0
votes
0
replies
299
views
How to subsample ATAC fragment file?
single-cell
atac-seq
scRNA-seq
updated 21 days ago by
Ram
43k • written 6 months ago by
bioinfo
▴ 150
0
votes
0
replies
677
views
Comment:
Comment: How to assign gene names after kallisto when I add GFP?
6 months ago by
bioinfo
▴ 150
0
votes
1
reply
677
views
Comment:
Comment: How to assign gene names after kallisto when I add GFP?
6 months ago by
bioinfo
▴ 150
0
votes
2
replies
1.3k
views
Removing constant/zero columns for PCA?
R
pca
updated 6 months ago by
Mensur Dlakic
★ 27k • written 6 months ago by
bioinfo
▴ 150
1
vote
4
replies
677
views
How to assign gene names after kallisto when I add GFP?
tximport
RNA-seq
kallisto
6 months ago by
bioinfo
▴ 150
0
votes
0
replies
1.8k
views
Comment:
Comment: How to plot proportion of cells in each cluster with scanpy?
7 months ago by
bioinfo
▴ 150
0
votes
0
replies
1.8k
views
Comment:
Comment: How to plot proportion of cells in each cluster with scanpy?
7 months ago by
bioinfo
▴ 150
1
vote
8
replies
1.8k
views
How to plot proportion of cells in each cluster with scanpy?
scRNA-seq
scanpy
single-cell
7 months ago by
bioinfo
▴ 150
0
votes
1
reply
1.8k
views
Comment:
Comment: How to plot proportion of cells in each cluster with scanpy?
7 months ago by
bioinfo
▴ 150
0
votes
1
reply
1.8k
views
Comment:
Comment: How to plot proportion of cells in each cluster with scanpy?
7 months ago by
bioinfo
▴ 150
0
votes
0
replies
649
views
Comment:
Comment: How to calculate GC content of reads that mapped to a specific gene?
7 months ago by
bioinfo
▴ 150
5
votes
2
replies
649
views
How to calculate GC content of reads that mapped to a specific gene?
STAR
RNA-seq
7 months ago by
bioinfo
▴ 150
0
votes
0
replies
890
views
Comment:
Comment: Can the DESeq2 object for paired data be set with design= ~ batch + condition?
7 months ago by
bioinfo
▴ 150
0
votes
1
reply
890
views
Comment:
Comment: Can the DESeq2 object for paired data be set with design= ~ batch + condition?
7 months ago by
bioinfo
▴ 150
0
votes
0
replies
890
views
Comment:
Comment: Can the DESeq2 object for paired data be set with design= ~ batch + condition?
7 months ago by
bioinfo
▴ 150
0
votes
1
reply
890
views
Comment:
Comment: Can the DESeq2 object for paired data be set with design= ~ batch + condition?
7 months ago by
bioinfo
▴ 150
0
votes
8
replies
890
views
Can the DESeq2 object for paired data be set with design= ~ batch + condition?
rna-seq
deseq2
7 months ago by
bioinfo
▴ 150
1
vote
1
reply
568
views
Do I need to perform basic filtering before using scrublet?
scanpy
scrublet
updated 8 months ago by
GenoMax
141k • written 8 months ago by
bioinfo
▴ 150
0
votes
0
replies
930
views
Comment:
Comment: Questions about per base sequence quality and GC content.
8 months ago by
bioinfo
▴ 150
0
votes
1
reply
930
views
Comment:
Comment: Questions about per base sequence quality and GC content.
8 months ago by
bioinfo
▴ 150
0
votes
0
replies
958
views
Comment:
Comment: How to choose threshold for scrublet?
8 months ago by
bioinfo
▴ 150
0
votes
2
replies
958
views
How to choose threshold for scrublet?
rna-seq
scrublet
8 months ago by
bioinfo
▴ 150
0
votes
0
replies
930
views
Comment:
Comment: Questions about per base sequence quality and GC content.
8 months ago by
bioinfo
▴ 150
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