This is a test version of Biostars. For the public version, visit https://www.biostars.org.
a.james
a.james
Reputation:
240 (Trusted)
Joined:
12.2 years ago
Last seen:
5.6 years ago
Location:
Switzerland
Latest posts by user
1 vote
0 replies
0 views
Comment: C: How to perform the lncRNA enrichment analysis?
written by a.james 24
0 votes
0 replies
0 views
Comment: C: List of TCGA genes differentially expressed in normal versus tumor
written by a.james 24
0 votes
0 replies
1.4K views
How to get the refSNP ids or rsIDs of variants from UKbiobank datasets
snp sequencing genome next-gen
written by a.james 24
0 votes
0 replies
0 views
Comment: C: Download the promoter, enchancer, TSS , 3 prime, exon and intron positions of al
written by a.james 24
0 votes
4 replies
3.9K views
Download the promoter, enchancer, TSS , 3 prime, exon and intron positions of all hg38 genes
rna-seq dna-seq
updated by Lhl 76 • | written by a.james 24
0 votes
1 reply
863 views
how to extact first 100 lines of an indexed BED file
bed genome
written by a.james 24
0 votes
0 replies
1.0K views
How to annotate illumina HumanHT-12_V3_0_R3_11283641_A.txt data
genome illumina array
written by a.james 24
0 votes
0 replies
0 views
Comment: C: Tools for predicting the protein altering effects of the variants from EXON-seq
written by a.james 24
0 votes
2 replies
1.6K views
Tools for predicting the protein altering effects of the variants from EXON-seq data
exon-seq variants snp sequencing
written by a.james 24
0 votes
1 reply
1.1K views
Finding the coverage of variants from variant file, which has no DF4 field
assembly rna-seq
written by a.james 24
0 votes
1 reply
0 views
Comment: C: The Picard FilterSAM READ is throwing error
written by a.james 24
0 votes
3 replies
2.5K views
The Picard FilterSAM READ is throwing error
rna-seq picard assembly reads
updated by Pierre Lindenbaum 17K • | written by a.james 24
0 votes
1 reply
0 views
Comment: C: Finding the best alignment from a paternal and maternal BAM file
written by a.james 24
0 votes
3 replies
1.6K views
Finding the best alignment from a paternal and maternal BAM file
rna-seq
updated by Carlo Yague 906 • | written by a.james 24
0 votes
0 replies
0 views
Comment: C: Extracting the reads counts (coverage) a specific variant allele from a Fastq fi
written by a.james 24
0 votes
1 reply
0 views
Comment: C: Extracting the reads counts (coverage) a specific variant allele from a Fastq fi
written by a.james 24
0 votes
4 replies
1.9K views
Extracting the reads counts (coverage) a specific variant allele from a Fastq file
rna-seq snp sequencing
written by a.james 24
0 votes
1 reply
0 views
Comment: C: How to retrieve metadata from the manifest data and UUID from genomic data commo
written by a.james 24
1 vote
1 reply
0 views
Comment: C: Sample names for TCGA data from GDC-legacy archive
written by a.james 24
0 votes
1 reply
0 views
Comment: C: Sample names for TCGA data from GDC-legacy archive
written by a.james 24
Latest awards to user
TODO: Awards