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3
votes
3
replies
1.0k
views
What are accession numbers starting with PIR e.g. PIR60289?
GeneHancer
updated 4 months ago by 44k • written 2.9 years ago by ▴ 380
3
votes
5
replies
2.5k
views
What kind of systematic bias of sequencing data the following normalization procedure address?
next-gen normalization bias
updated 6.2 years ago by 44k • written 8.8 years ago by ▴ 380
30
votes
9
replies
28k
views
samtools bedcov vs. bedtools coverage
DNA-seq coverage
updated 6.3 years ago by 44k • written 8.5 years ago by ▴ 380
20
votes
16
replies
6.2k
views
Breaking down the reference genome chromosome-wise
reference-genome fasta
updated 4 months ago by 44k • written 10.1 years ago by ▴ 380
0
votes
3
replies
3.5k
views
How to create a pooled normal exome sample?
copy-number-analysis exome next-gen-sequencing
updated 24 months ago by 44k • written 9.5 years ago by ▴ 380
0
votes
0
replies
2.2k
views
Best way to normalize Human BodyMap 2.0 data
RNA-Seq normalization
updated 2.3 years ago by 44k • written 9.1 years ago by ▴ 380
5
votes
5
replies
4.2k
views
what does Num_Probes in a segmentation file refer to?
sequencing
updated 8.7 years ago by ★ 3.0k • written 8.7 years ago by ▴ 380
19
votes
15
replies
8.2k
views
6 follow
What is the best way to make a bam file smaller by removing unwanted information?
bam next-gen-sequencing
updated 2.4 years ago by 44k • written 8.9 years ago by ▴ 380
6
votes
5
replies
5.2k
views
How to create B-allele frequency file for ADTEx?
adtex next-gen-sequencing
updated 24 months ago by 44k • written 9.5 years ago by ▴ 380
11
votes
1
reply
5.0k
views
Does one need to sort and index after performing a rmdup in Samtools?
sequencing alignment samtools variant
updated 2.6 years ago by 44k • written 9.8 years ago by ▴ 380
2
votes
1
reply
3.1k
views
Estimating the expected number of reads that overlap a [heterozygous] snp in one window from the read depth, read length and resolution
statistics allele simualtion snp baf
updated 2.9 years ago by 44k • written 10.2 years ago by ▴ 380
6
votes
7
replies
2.9k
views
Why is the noise level higher in regions with amplification than regions with deletion in the genome?
snp dna-seq allele-fraction
updated 17 months ago by 44k • written 10.4 years ago by ▴ 380
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