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794 results • Page
2 of 16
Sort: replies
Rank
Views
Votes
Replies
4
votes
9
replies
2.2k
views
6 follow
Same sequencing sample in multiple lanes. How to analyse it?
sequencing
bowtie2
alignment
samtools
ngs
updated 13 days ago by
ST
• 0 • written 2.2 years ago by
Federico
• 0
4
votes
9
replies
2.7k
views
Tool:
CANEapp, a user-friendly application for automated next generation transcriptomic data analysis
RNA-Seq
written 8.3 years ago by
dvelmeshev
• 0
3
votes
9
replies
613
views
Is it Acceptable to Have Uniform Quality Scores in a FASTQ File?
FASTQ
updated 22 days ago by
Istvan Albert
100k • written 24 days ago by
Κοσμάς
• 0
11
votes
9
replies
7.1k
views
How to choose method to integrate different patient sample together in Seurat
Seurat
scRNA
batch-effect
harmony
updated 29 days ago by
Ram
43k • written 4.3 years ago by
623202215
▴ 80
0
votes
9
replies
342
views
Duplicated reads (IDs) from nanopore sequencing
bam
nanopore
sequencing
1 day ago by
njornet
▴ 20
0
votes
8
replies
451
views
Different output for read length
samtools
BAM
7 days ago by
marco.barr
▴ 130
3
votes
8
replies
592
views
How to access TCGA samples that were treated with a specific drug?
TCGA
RNA-seq
10 days ago by
Qroid
▴ 40
3
votes
8
replies
4.2k
views
Using FPKM and TPM values for batch correction for Single Cell RNA-Seq
fpkm
scRNA-seq
RNA-Seq
tpm
batch-effect
updated 28 days ago by
Ram
43k • written 4.6 years ago by
hkarakurt
▴ 180
8
votes
8
replies
750
views
PCA plot (Suggestions Needed)
DESeq2
PCAplot
updated 22 days ago by
swbarnes2
14k • written 23 days ago by
Aaliya
▴ 10
3
votes
8
replies
5.0k
views
An idea to identify batch effects
microarray
batch-effect
updated 28 days ago by
Ram
43k • written 9.7 years ago by
mjarosz
• 0
0
votes
8
replies
459
views
Error in cnetplot enrichplot package
R
updated 24 days ago by
Ram
43k • written 24 days ago by
Farhad
• 0
1
vote
8
replies
3.5k
views
Best way to address different batches of RNA-seq
sequence
RNA-Seq
RPKM
Fold-Change
batch-effect
updated 29 days ago by
Ram
43k • written 7.1 years ago by
tud55122
▴ 20
0
votes
8
replies
528
views
What does it mean single base resolution in sequencing?
SNP
sequencing
updated 16 days ago by
LauferVA
4.2k • written 18 days ago by
jinyu
▴ 10
2
votes
8
replies
377
views
joint callset and vcf sorting, unknown TAG issue
sort
bcftools
GLNexus
merge
VCF
updated 4 days ago by
Pierre Lindenbaum
161k • written 5 days ago by
Matteo Ungaro
▴ 100
1
vote
8
replies
945
views
Adding CB tag to bam file
samtools
bam
updated 22 days ago by
Pierre Lindenbaum
161k • written 28 days ago by
Maria
• 0
4
votes
8
replies
763
views
Create a new bed file with all pairwise combinations between two other bed files, based on bp distance
SNPs
BED
eqtl
bedtools
updated 20 days ago by
Alex Reynolds
35k • written 21 days ago by
J
▴ 10
3
votes
8
replies
6.6k
views
7 follow
GATK genomicsDBimport intervals for WGS
gatk
genomicsdbimport
updated 14 days ago by
Sd
• 0 • written 5.1 years ago by
Nicolas Rosewick
11k
1
vote
8
replies
542
views
Downsampling fastq file
downsample
fastq
16 days ago by
marco.barr
▴ 130
3
votes
8
replies
679
views
Spike-in control found in raw reads (16S amplicon seq) but not picked up by DADA2 - where to go from here?
nf-core
16S
amplicon
dada2
ampliseq
updated 10 days ago by
Chris Dean
▴ 410 • written 14 days ago by
sovrappensiero
▴ 100
3
votes
8
replies
1.4k
views
Cellranger count error: Input FASTQ file ended prematurely
scRNA-seq
Cellranger
STARsolo
10X
updated 27 days ago by
swbarnes2
14k • written 9 months ago by
bp22
▴ 80
6
votes
7
replies
385
views
Longest transcript variant per gene
transcript
longest
variant
orthofinder
4 days ago by
sansan_96
▴ 90
3
votes
7
replies
409
views
FastQC Quality per tile and per sequence behaving strange after using Cutadapt
fastqc
cutadapt
illumina
tile
paired-end
17 days ago by
salias
• 0
4
votes
7
replies
632
views
Very low RNA splicing rate for pulmonary AT2 cells
RNA-velocity
scVelo
scRNA-seq
splicing
17 days ago by
e.r.zakiev
▴ 210
1
vote
7
replies
380
views
Overlapping Ranges within Granges object
Genomicranges
IRanges
GRanges
2 days ago by
ntsopoul
▴ 60
2
votes
7
replies
1.4k
views
6 follow
Differential Expression using Isoseq-supplemented reference transcriptome
RNA-Seq
Salmon
Isoseq
updated 18 days ago by
Gordon Smyth
★ 7.2k • written 8 months ago by
Calum
▴ 10
0
votes
7
replies
74
views
zero TPM for many gene including housekeeping when using kallisto
RNAseq
updated just now by
ATpoint
82k • written 2 hours ago by
ashkan
▴ 160
4
votes
7
replies
408
views
How does gene length effect the number of reads mapped
RNA-seq
CPM
sequencing
3 days ago by
Chen
• 0
7
votes
7
replies
6.0k
views
6 follow
How to know synonymous and non-synonymous SNPs from transcriptome sequencing
RNA-Seq
SNP
updated 21 days ago by
rohitsatyam102
▴ 860 • written 6.2 years ago by
smallfish
▴ 10
0
votes
7
replies
428
views
RNAseq one control two conditions, shared and exclusive genes
conditions
RNAseq
multiple
Rstudio
updated 4 days ago by
Mohamed Abderrahmane
▴ 20 • written 18 days ago by
matteo.levorato
• 0
1
vote
7
replies
536
views
Question regarding WGCNA
WGCNA
Network-construction
7 days ago by
deepak
• 0
1
vote
7
replies
609
views
gvcf joint calling
WES
GATK
VCF
gVCF
19 days ago by
zihanss
• 0
6
votes
7
replies
1.6k
views
How to assess RNA-Seq batch correction success?
Combat
RNA-Seq
Limma
DESeq2
batch-effect
updated 28 days ago by
Ram
43k • written 5.0 years ago by
borkk
▴ 140
5
votes
7
replies
485
views
RNA seq analysis
DESeq
RNA-seq
2 days ago by
Jacek
▴ 20
0
votes
7
replies
635
views
Post-imputation plot
michigan-imputation-server
quality-control
updated 14 days ago by
LChart
3.9k • written 17 days ago by
kl
▴ 10
4
votes
7
replies
604
views
To get p-values for the TPM
P-value
TPM
RSEM
updated 22 days ago by
dsull
★ 6.0k • written 23 days ago by
VITALA
• 0
9
votes
7
replies
7.2k
views
Align paired and unpaired reads simultaneously using Bowtie2?
alignment
updated 6 days ago by
Ruqaiya
• 0 • written 5.7 years ago by
xiaozhongzhiping
▴ 20
2
votes
7
replies
5.3k
views
6 follow
Memory usage of picard Samsort
Picard
SortSam
updated 27 days ago by
ATpoint
82k • written 7.2 years ago by
boymin2020
▴ 80
3
votes
7
replies
315
views
Faster Needleman-Wunsch rapid global alignment of two sequences?
Needleman-Wunsch
alignment
updated 5 hours ago by
DGTool
▴ 20 • written 23 hours ago by
Gabriel R.
★ 2.9k
0
votes
7
replies
1.9k
views
Batch effect correction in RNASeq data and plot Dendrograms cluster
clustering
dendrogram
RNA-Seq
batch-effect
updated 28 days ago by
Ram
43k • written 4.1 years ago by
Ankit
▴ 500
2
votes
7
replies
942
views
Removing duplicates
duplicates
ONT
minimap2
updated 28 days ago by
noodle
▴ 580 • written 4 weeks ago by
quentinperriere
• 0
1
vote
7
replies
608
views
ScRNA data question
scRNA
Vlnplot
Samples
updated 17 days ago by
bk11
★ 2.5k • written 21 days ago by
starswillfade
▴ 10
3
votes
7
replies
1.0k
views
Can I use batch effect correction "by parts"?
ComBat
RNA-Seq
batch-effect
updated 29 days ago by
Ram
43k • written 4.4 years ago by
n,n
▴ 360
1
vote
7
replies
496
views
Downsampling long-read BAM files
nanopore
BAM
QC
ONT
downsampling
14 days ago by
eebloom
▴ 80
0
votes
6
replies
473
views
Differential Expression Analysis using DESeq2 in R
deseq2
R
updated 13 days ago by
swbarnes2
14k • written 13 days ago by
Erina
• 0
3
votes
6
replies
752
views
Ciriquant not configuring hisat2 indexed files
ciriquant
25 days ago by
Atul K.
• 0
0
votes
6
replies
2.1k
views
Copy number Variation analysis using conumee
R
software error
sequencing
genome
updated 8 days ago by
GenoMax
142k • written 3.2 years ago by
gs000095
▴ 10
0
votes
6
replies
445
views
How to slice a gvcf file with tabix?
Tabix
bed
gvcf
23 days ago by
Sd
• 0
7
votes
6
replies
1.3k
views
using different microarray datasets (meta-analysis?) for DEG pipeline
microarray
meta-analysis
DEG
batch-effect
updated 29 days ago by
Ram
43k • written 4.9 years ago by
mosesoo
▴ 30
4
votes
6
replies
4.0k
views
Correcting for batch effect in RNA-seq data
RNA-Seq
batch-effect
updated 29 days ago by
Ram
43k • written 4.8 years ago by
Rimma
▴ 30
0
votes
6
replies
419
views
Is it Possible to "Merge" data from Replicates within a VCF SNP File
snp
vcf
genomics
plink
updated 3 days ago by
Ram
43k • written 6 days ago by
ajbarrett98
• 0
794 results • Page
2 of 16
Recent Votes
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
Answer: In one PCA plot, can I calculate the percentage of different factors that contri
Answer: In one PCA plot, can I calculate the percentage of different factors that contri
Answer: Details on salmon index
Answer: Generating consensus sequence from bam file
Answer: Short Read Data Genome Assembly
Comment: API kegg - IndexError: list index out of range
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Comment: zero TPM for many gene including housekeeping when using kallisto
by
ATpoint
82k
Yes, but this is what I am saying: GAPDH in human has at least 6 annotated transcripts. Have you looked at all of them? Maybe that particul…
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@atpoint these are from PBMC. no they are different genes. for example ENST00000229239.10 is GAPDH. in STAR I got a lot of reads aligned …
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@dariober: I have to use kallisto for our downstream pipeline.
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ATpoint
82k
Which celltype is this? Are these transcripts of the same gene, and of which gene?
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ashkan
▴ 160
@atpoint the question is updated. the first command shows how the index is built.
Comment: Help! Reconstruction of locus, order contigs
by
dthorbur
★ 2.0k
Is the *de novo* annotation required for each contig? Reconstructing homologous regions in many genomes can be tricky regardless, but is es…
Comment: In one PCA plot, can I calculate the percentage of different factors that contri
by
diqixiaoyaoer
▴ 20
You can have a look on my answer. I have post it below.
Answer: In one PCA plot, can I calculate the percentage of different factors that contri
by
diqixiaoyaoer
▴ 20
Here is my script that can be used to calculate how much degree that different factors contribute to PCA variance (PC1 and PC2). # …
Comment: Details on salmon index
by
Lorenzo
• 0
Thank you so much for the beautiful explanation. Just one more curiosity. So in the first versions Salmon utilized RapMap to index and then…
Comment: What marks a De-Novo Genome assembly as FAILED?
by
dthorbur
★ 2.0k
I'm a little confused about your experimental design. Are you making 45 different assemblies? Or are all the samples from the same individu…
Comment: zero TPM for many gene including housekeeping when using kallisto
by
ATpoint
82k
You should be stating how you constructed the index, and include the actual lines for the problematic genes from the abundance files. Note …
Comment: zero TPM for many gene including housekeeping when using kallisto
by
dariober
14k
You could try [salmon](https://combine-lab.github.io/salmon/getting_started/) to see if the problem is with kallisto or with the pseudo-ali…
Comment: solution-Transcriptome.cpp:18:Transcriptome: exiting because of *INPUT FILE* err
by
GenoMax
142k
> INPUT FILE error: could not open input file /geneInfo.tab Based on the error it appears that the input file you are providing could not …
Answer: How to handle duplicated genes in TCGA data?
by
txema.heredia
▴ 130
Having duplicate gene symbols is pretty common. Why do you need to work with gene symbols? To compare them to external datasets? Or just fo…
Comment: Merge clusters in Seurat UMAP
by
kilcdincer
▴ 10
It did not help either. But I got the answer [here][1] Thank you! [1]: https://github.com/satijalab/seurat/issues/8902
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