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Comment:
C: [Crushing the bureaucracy in bioinformatics] Introducing Skymap-JupyterHub: acce
6.3 years ago by
btsui
▴ 300
11
votes
10
replies
2.6k
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Tool:
[Crushing the bureaucracy in bioinformatics] Introducing Skymap-JupyterHub: accessing and utilizing reprocessed expression/ allelic read count profil…
SNP
RNA-Seq
ChIP-Seq
updated 20 months ago by
Ram
44k • written 6.5 years ago by
btsui
▴ 300
1
vote
0
replies
1.4k
views
Comment:
C: Text mining in PDFs
6.4 years ago by
btsui
▴ 300
0
votes
1
reply
3.6k
views
Answer:
A: Extract start coordinate from read 1 and end coordinate from read 2 of paired en
updated 6.5 years ago by
finswimmer
16k • written 6.5 years ago by
btsui
▴ 300
0
votes
0
replies
973
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Comment:
C: Is it correct to pool transcriptomes coming from different experiment for DE ana
6.5 years ago by
btsui
▴ 300
0
votes
1
reply
2.6k
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Comment:
C: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing
6.5 years ago by
btsui
▴ 300
0
votes
2
replies
2.6k
views
Comment:
C: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing
6.5 years ago by
btsui
▴ 300
0
votes
1
reply
2.3k
views
Comment:
C: Copy number differences between groups
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
3.0k
views
Answer:
A: Tool that can split genes into groups with similar expression pattern overtime
6.5 years ago by
btsui
▴ 300
0
votes
1
reply
6.4k
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Comment:
C: How to normalize count data for PCA in R - something goes wrong
6.5 years ago by
btsui
▴ 300
0
votes
1
reply
2.3k
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Answer:
A: Allele counting tool for a list of known indels from paired end sequencing data
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
7.5k
views
Comment:
C: TCGA expression data (TPM)
6.5 years ago by
btsui
▴ 300
0
votes
1
reply
3.2k
views
Comment:
C: how to detect mutation from viral RNA-seq data
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
1.5k
views
Comment:
C: Probabilistic PCA on very sparse SNP matrix
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
1.7k
views
Answer:
A: Grail: reflow on AWS vs others (snakemake/cfncluster, etc)
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
1.5k
views
Comment:
C: TACC vs SDSC vs HTCondor
6.5 years ago by
btsui
▴ 300
1
vote
2
replies
1.5k
views
Comment:
C: TACC vs SDSC vs HTCondor
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
1.5k
views
Blog:
Buying computing infrastructure vs adopting the Cloud in Bioinformatics
sequence
updated 2.0 years ago by
Ram
44k • written 6.5 years ago by
btsui
▴ 300
0
votes
0
replies
3.2k
views
Comment:
C: How to detect segmental duplications?
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
1.2k
views
Comment:
C: Best technique for CNV and mutation analysis
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
841
views
Answer:
A: How to automatically retrieve genes of preselected enzymes in a pathway map?
6.5 years ago by
btsui
▴ 300
2
votes
0
replies
6.9k
views
Comment:
C: Design in DESeq: Can you combine explicit and implicit batch effect correction i
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
1.4k
views
Comment:
C: Estimating the purity of tumor cells in microarray data
6.5 years ago by
btsui
▴ 300
1
vote
1
reply
1.5k
views
Answer:
A: Mapping metagenome information to amplicon sequences
6.5 years ago by
btsui
▴ 300
2
votes
0
replies
1.6k
views
Answer:
A: Variant Allele Frequency
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
990
views
Answer:
A: GEO search filtering
6.5 years ago by
btsui
▴ 300
1
vote
0
replies
7.2k
views
Answer:
A: Adjusting for confounding variables in RNA-SEQ Differential Expression Analysis
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
2.6k
views
Comment:
A: Programmatically retrieve the length of a gene
6.5 years ago by
btsui
▴ 300
2
votes
0
replies
2.1k
views
Answer:
A: Assembly of wheat genome
6.5 years ago by
btsui
▴ 300
2
votes
0
replies
1.0k
views
Answer:
A: make a new bam file
6.5 years ago by
btsui
▴ 300
3
votes
0
replies
2.5k
views
Answer:
A: GWAS summary file including risk allele, protective allele and disease
6.5 years ago by
btsui
▴ 300
0
votes
0
replies
2.6k
views
Comment:
C: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing
6.5 years ago by
btsui
▴ 300
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