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0
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Comment: C: HLA-DRB1 variant name description
10.2 years ago by lh3 33k
0
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0
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8.1k
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Comment: C: Why the CEU trio's parents NA12891 and NA12892 are not in 1000 Genomes phase 3
10.2 years ago by lh3 33k
0
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2
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8.1k
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Comment: C: Why the CEU trio's parents NA12891 and NA12892 are not in 1000 Genomes phase 3
10.2 years ago by lh3 33k
1
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1
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6.9k
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Comment: C: ion torrent alignment software
10.2 years ago by lh3 33k
4
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1
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8.1k
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Answer: Answer: Why the CEU trio's parents NA12891 and NA12892 are not in 1000 Genomes phase 3
updated 3.2 years ago by 45k • written 10.2 years ago by 33k
0
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1
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3.2k
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Comment: C: Effect of indel mutation on protein
10.2 years ago by lh3 33k
1
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0
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9.1k
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Comment: C: bioawk installation issue "command not found"
10.2 years ago by lh3 33k
1
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1
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3.2k
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Comment: Comment: Effect of indel mutation on protein
updated 3.2 years ago by 45k • written 10.2 years ago by 33k
2
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1
reply
6.4k
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Comment: C: parsing BAM index (quick&dirty samtools view X.bam region)
10.2 years ago by lh3 33k
0
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0
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3.0k
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Comment: C: Effect of Read Length?
10.2 years ago by lh3 33k
0
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0
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8.2k
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Comment: C: Perl6 and the Future of Bioinformatics - Compatibility and Integration
10.2 years ago by lh3 33k
0
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0
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5.5k
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Comment: C: Aligner for super-short sequences
10.2 years ago by lh3 33k
0
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1
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6.2k
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Comment: C: Is that possible to use Neighbor Joining algorithm for a distance matrix with mo
10.2 years ago by lh3 33k
0
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1
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6.2k
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Comment: C: Is that possible to use Neighbor Joining algorithm for a distance matrix with mo
10.2 years ago by lh3 33k
0
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1
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6.2k
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Comment: C: Is that possible to use Neighbor Joining algorithm for a distance matrix with mo
10.2 years ago by lh3 33k
1
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2
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6.2k
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Comment: C: Is that possible to use Neighbor Joining algorithm for a distance matrix with mo
10.2 years ago by lh3 33k
0
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0
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38k
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Comment: C: Help a graduate student going into Bioinformatics looking for a new personal lap
10.2 years ago by lh3 33k
0
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1
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38k
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Comment: C: Help a graduate student going into Bioinformatics looking for a new personal lap
10.2 years ago by lh3 33k
0
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0
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2.7k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
10.3 years ago by lh3 33k
2
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1
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2.7k
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Comment: C: Read depths from 1000G exome sequencing are almost all zero.
10.3 years ago by lh3 33k
2
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1
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5.4k
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Answer: A: 1000 Genome Derived Allele Frequency
10.3 years ago by lh3 33k
0
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1
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2.3k
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Comment: C: De novo mutation rate per base pair
10.3 years ago by lh3 33k
0
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0
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6.0k
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Comment: C: Hardy-Weinberg assumptions in variant calling
10.3 years ago by lh3 33k
5
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2
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6.0k
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Answer: A: Hardy-Weinberg assumptions in variant calling
10.3 years ago by lh3 33k
2
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1
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3.2k
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Comment: C: Sam Reference sequence length does not match with the actual fasta sequence inpu
10.3 years ago by lh3 33k
1
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0
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6.2k
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Comment: C: Google genomics cloud platform ?
10.4 years ago by lh3 33k
0
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1
reply
6.7k
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Comment: C: Convert VCF to BCF
10.4 years ago by lh3 33k
1
vote
1
reply
22k
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Comment: C: Error while running BWA mem
10.4 years ago by lh3 33k
0
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1
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22k
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Comment: C: Error while running BWA mem
10.4 years ago by lh3 33k
1
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0
replies
5.7k
views
Comment: Comment: Which Tools do you use for (Tandem) Repeat Detection? Why?
updated 2.9 years ago by 45k • written 10.4 years ago by 33k
1
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0
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2.8k
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Comment: Comment: Haplotype Reference consortium Release!
updated 2.9 years ago by 45k • written 10.4 years ago by 33k
1
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1
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2.8k
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Comment: Comment: Fetch a single chromosome from a WGS bam located on an object store
updated 2.9 years ago by 45k • written 10.4 years ago by 33k
2
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1
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2.8k
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Comment: C: Fetch a single chromosome from a WGS bam located on an object store
10.4 years ago by lh3 33k
0
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1
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8.6k
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Comment: Comment: How to handle chr Y data in BAM files from exome sequencing of human females
updated 2.9 years ago by 45k • written 10.4 years ago by 33k
2
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1
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8.6k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
10.4 years ago by lh3 33k
0
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0
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3.3k
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Comment: C: What does this mean in my read (samtools)
10.4 years ago by lh3 33k
0
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0
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14k
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Comment: C: Split Read in Samtools
10.4 years ago by lh3 33k
0
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0
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29k
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Comment: C: How to determine reference genome that was used for alignment given BAM with obs
10.4 years ago by lh3 33k
0
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1
reply
14k
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Comment: C: Split Read in Samtools
10.4 years ago by lh3 33k
0
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1
reply
14k
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Comment: C: Split Read in Samtools
10.4 years ago by lh3 33k
2
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0
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29k
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Comment: C: How to determine reference genome that was used for alignment given BAM with obs
10.4 years ago by lh3 33k
0
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0
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4.9k
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Comment: C: Is the readlenght of BGI/ CompleGenomics Revolocity long enough to compete with
10.4 years ago by lh3 33k
2
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0
replies
2.3k
views
Comment: Comment: [internship project] condition where BLAST > BWA.
updated 2.9 years ago by 45k • written 10.5 years ago by 33k
8
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1
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2.0k
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Answer: C: Fastq size: Why don't we have nucleotide information merged to quality scores?
10.5 years ago by lh3 33k
0
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0
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61k
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Comment: Comment: how to unzip the files in batch?
updated 2.9 years ago by 45k • written 10.5 years ago by 33k
24
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2
replies
31k
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Answer: Answer: Remove duplicates in fasta file based on ID
updated 2.8 years ago by 45k • written 10.5 years ago by 33k
3
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1
reply
3.1k
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Comment: Comment: No more hidden solutions in bioinformatics
updated 2.8 years ago by 45k • written 10.5 years ago by 33k
1
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0
replies
3.0k
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Comment: C: Looking for information on designing effective accession numbers.
10.5 years ago by lh3 33k
1
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0
replies
3.0k
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Comment: Comment: Looking for information on designing effective accession numbers.
updated 2.9 years ago by 45k • written 10.5 years ago by 33k
1
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0
replies
11k
views
Comment: Comment: Best bioinfo one-liners?
updated 2.9 years ago by 45k • written 10.5 years ago by 33k
1,458 results • Page 6 of 30
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