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187 results • Page
4 of 4
Sort: Views
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Views
Votes
Replies
0
votes
1
reply
113
views
No output when converting transcript IDs to gene symbols
RNA-seq
updated 18 hours ago by
Ram
44k • written 1 day ago by
ashkan
▴ 160
0
votes
1
reply
110
views
Small secondary peak for per sequence GC content - FASTQC results (bulk RNA-seq)
RNAseq
updated 18 hours ago by
GenoMax
142k • written 18 hours ago by
Fossil
• 0
0
votes
0
replies
108
views
DIFFBIND boxplot results, p value not significant
DiffBind
ChIP-seq
22 hours ago by
RD
▴ 10
0
votes
1
reply
106
views
How to hide label in layout file of MCscan (python version)
MCscan
updated 3 days ago by
GenoMax
142k • written 3 days ago by
jinyi
• 0
0
votes
0
replies
105
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
104
views
Linking AMR Genes to Taxonomy in Soil Metagenomics
metagenomics
bacteria
wgs
AMR
resistome
updated 1 day ago by
GenoMax
142k • written 1 day ago by
LuciaNhu
• 0
0
votes
0
replies
104
views
transcriptome annotation
annotation
trinity
transcriptome
updated 2 days ago by
Ram
44k • written 3 days ago by
Asim Bin Arshad
• 0
0
votes
0
replies
103
views
Challenges of Affymetrix probe IDs for grouping similar genes to calculate their mean
R
Mean
Affymetrix
Probes
Grouping
3 days ago by
Maryam
• 0
0
votes
0
replies
98
views
Is it possible to keep gene_id and gene_name columns using Seurat::Read10X?
Seurat
single-cell
scRNA-seq
updated 2 days ago by
Ram
44k • written 3 days ago by
ev97
▴ 20
0
votes
0
replies
97
views
MAFFT alignment report
RNA
Alignment
MAFFT
Linux
updated 18 hours ago by
Ram
44k • written 1 day ago by
Ghada
• 0
0
votes
0
replies
97
views
Kegg Pathways to Circos
Genomics
KEGG
Circos
1 day ago by
dlera.lozano
▴ 10
0
votes
0
replies
96
views
News:
Online course: Network analysis in Systems Biology with R/Bioconductor
Bioconductor
Systems-Biology
Network-Analysis
R
updated 2 days ago by
Ram
44k • written 2 days ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
95
views
Flag multiple filtering steps on VCF files using VEP
FILTERING
VEP
VCF
updated 17 hours ago by
Pierre Lindenbaum
162k • written 17 hours ago by
avelarbio46
▴ 30
0
votes
0
replies
93
views
News:
Online course- Advanced Python for Life Sciences
Python-Programming
Data-Visualisation
Machine-Learning
updated 1 day ago by
Ram
44k • written 2 days ago by
carlopecoraro2
★ 2.5k
1
vote
4
replies
88
views
Error with BiocParallel. No barcodes files found
Barcodes
scRNA-seq
SingleCellExperiment
57 minutes ago by
NTerway
• 0
0
votes
0
replies
90
views
Last step of metagenome analysis before visualization
metagenome
python
analyis
2 days ago by
Ayda Ecem
• 0
1
vote
2
replies
88
views
How to interpret this plotMDS of three disease clusters?
microarray
plotMDS
DEGs
updated 2 hours ago by
ATpoint
82k • written 4 hours ago by
egascon
• 0
0
votes
0
replies
88
views
Calculated LAI is too large
annotation
LAI
assembly
TE
genome
2 days ago by
Yao
▴ 30
0
votes
0
replies
88
views
How to recover the entire sequence from all_contig_annotations.csv?
VDJ
single-cell
TCR-seq
cellranger
10x
2 days ago by
dawnyipingzou
• 0
0
votes
0
replies
86
views
Rescaling normalized enrichment score (NES)
heatmap
1 day ago by
CTLong
▴ 110
0
votes
0
replies
86
views
News:
Bioinformatic Analysis of Transposable Elements course
Genome-Annotation
TE
Manual-Curation
Transposable-Elements
updated 18 hours ago by
Ram
44k • written 1 day ago by
carlopecoraro2
★ 2.5k
0
votes
0
replies
85
views
KEGG pathway enrichment analysis in Zea mays with R
KEGG
Zea-mays
R
updated 18 hours ago by
Ram
44k • written 23 hours ago by
letizia.ottaviani
• 0
0
votes
0
replies
83
views
ENCORI or starBase : ceRNA data retrieval using Web API and curl
ceRNA
ENCORI
curl
microRNA
starBase
3 days ago by
V_Vibes
• 0
0
votes
0
replies
82
views
Subset of ATAC-seq peaks has high variance
atac-seq
edgeR
R
normalization
8 hours ago by
Tim
• 0
0
votes
1
reply
79
views
Free AI for R programming
Programming
R
updated 2 hours ago by
GenoMax
142k • written 6 hours ago by
mohamadzare6022
▴ 10
1
vote
2
replies
76
views
Unexpected read length from NGS
NGS
Illumina
updated 2 hours ago by
ATpoint
82k • written 4 hours ago by
QX
• 0
0
votes
0
replies
76
views
How to find nucleotide changes and the predicted effect when comparing two genomes
BLAST
alignment
updated 18 hours ago by
Ram
44k • written 21 hours ago by
Melissa
• 0
0
votes
0
replies
70
views
Cancer vs Normal Cell Classification Based on SNVs
cancer
17 hours ago by
dglad
• 0
0
votes
0
replies
64
views
Extracting haplotype-specific annotations from splicing graph
vg
10 hours ago by
Juhyun
• 0
0
votes
1
reply
62
views
Cellranger-multi : Demultiplexing and Analyzing 5’ Immune Profiling Libraries Pooled with Hashtags
5InmuneProfiling
nf-core
scRNAseq
cellranger-multi
Nextflow
updated 2 hours ago by
GenoMax
142k • written 5 hours ago by
azeu
• 0
0
votes
0
replies
61
views
Phyloseq returning black bars for plot_bar
phyloseq
bioconductor
R
14 hours ago by
Jacob
• 0
0
votes
0
replies
57
views
miloR - object 'as.SimpleList' of mode 'function' was not found when running calcNhoodDistance
scRNA-seq
seurat
miloR
10 hours ago by
shuaizh117
▴ 10
0
votes
0
replies
40
views
VEP annotation tool: "." isn't numeric in addition (+)
annotation
Variant
VEP
warning
VCF
4 hours ago by
emmanouil.a
▴ 120
0
votes
0
replies
35
views
GWAS or QTL mapping in RIL population
GWAS
RIL
4 hours ago by
韩雨
• 0
0
votes
0
replies
31
views
Tools for chromosomal aneuploidy detection
genetics
aneuploidy
NGS
human
2 hours ago by
adarsh_pp
▴ 40
0
votes
0
replies
27
views
Assigning Micro-C read pairs to nucleosomes called from MNase-seq data?
Hi-C
MNase-Seq
6 hours ago by
Linus
• 0
187 results • Page
4 of 4
Recent Votes
Comment: log2 fold change in RNA-seq analysis
Comment: log2 fold change in RNA-seq analysis
Answer: Ideal PC configurations and operating system for bioinformatics laboratory
correct way of analyzing cell proportions in singlecell data
Comment: How to interpret this plotMDS of three disease clusters?
gseGO: no term enriched under specific pvalueCutoff
Answer: Error with BiocParallel. No barcodes files found
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Recent Replies
Answer: Z score
by
Akash D
▴ 50
I made this. Z scored on log2FC? will anyone support me on this? 3 groups A,B,C
Comment: log2 fold change in RNA-seq analysis
by
i.sudbery
19k
There is no such thing as a fold change of -2. Fold change is expression_in_condition_A/expresssion_in_condition_B as expression is a…
Comment: Ideal PC configurations and operating system for bioinformatics laboratory
by
i.sudbery
19k
DE with 100s of samples (particulalry if your experiemental design is more complex than 2 condition DE) can stretch consumer grade hardware…
Comment: Error with BiocParallel. No barcodes files found
by
NTerway
• 0
Thank you for your help! I will try this out. I am trying to implement a collaborator's pipeline on my data and they only use SCE, scran an…
Comment: Ideal PC configurations and operating system for bioinformatics laboratory
by
ATpoint
82k
Once you have the counts any n is possible on a regular analysis-grade laptop or workstation. Even hundreds of samples. It's really the pre…
Comment: Error with BiocParallel. No barcodes files found
by
ATpoint
82k
You just tell the function to remove the prefix for you. Not on the actual file. Then you can add this information to the SCE, like `sce$da…
Comment: log2 fold change in RNA-seq analysis
by
May Ling
• 0
Thank you for your response. I apologize if my understanding is incomplete. I would like to ask: if I have a fold change of -2, how can I c…
Comment: Ideal PC configurations and operating system for bioinformatics laboratory
by
i.sudbery
19k
Yeah, a standard 3x3 bulk experiement is very analysable on pretty much most good consumer laptops these days.
Comment: Error with BiocParallel. No barcodes files found
by
NTerway
• 0
Thanks for the explanation! If I remove the prefix (GSM3972009_69_) then I will lose the sample annotation and cannot track them. I am more…
Comment: Unexpected read length from NGS
by
ATpoint
82k
Seconding this. Just ask them.
Answer: Error with BiocParallel. No barcodes files found
by
ATpoint
82k
The function assumes simply barcodes.tsv(.gz), genes.tsv(.gz) and matrix.mtx(.gz), without additional pre- or suffixes by default. You can …
Comment: Free AI for R programming
by
GenoMax
142k
Try: https://ai.tinybio.cloud/
Comment: How to interpret this plotMDS of three disease clusters?
by
ATpoint
82k
arrayWeights is imo always a good idea with human (or generally large) cohorts. What you can also do is to use something like sva to estima…
Comment: Cellranger-multi : Demultiplexing and Analyzing 5’ Immune Profiling Libraries Po
by
GenoMax
142k
Not what you want to hear but it is possible that the Ab data is not good quality as the cellranger message says (assuming everything ran p…
Comment: Ideal PC configurations and operating system for bioinformatics laboratory
by
ATpoint
82k
Bulk RNA-seq is way less intensive in every regard than single-cell. Whatever you buy, be sure it's upgradable, meaning, no Mac :)
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