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345
votes
94
replies
251k
views
59 follow
Tools To Calculate Average Coverage For A Bam File?
coverage
bam
sequencing
updated 12 weeks ago by
GenoMax
146k • written 13.8 years ago by
Biomed
5.0k
124
votes
13
replies
180k
views
13 follow
How Can I Convert Bam To Sam?
bam
next-gen-sequencing
sam
updated 14 months ago by
Ram
44k • written 14.3 years ago by
Biomed
5.0k
2
votes
2
replies
3.0k
views
What Is The Best Tool To Detect Ibd In A Trio (Mom, Dad, Child)
snp
updated 4.9 years ago by
Charles Warden
8.3k • written 13.1 years ago by
Biomed
5.0k
0
votes
0
replies
4.2k
views
Comment:
C: Affy Data Into Illumina Genome Studio
updated 5.2 years ago by
Ram
44k • written 14.5 years ago by
Biomed
5.0k
42
votes
6
replies
26k
views
6 follow
Can You Please Tell Me Where I Find Information About .Fai File Format?
maf
gatk
updated 5.3 years ago by
John Marshall
3.1k • written 14.4 years ago by
Biomed
5.0k
9
votes
2
replies
2.7k
views
What would be the expected average coverage of a 384 multiplexed run on a Novaseq S4 flowcell?
novaseq
coverage
updated 5.9 years ago by
ATpoint
85k • written 5.9 years ago by
Biomed
5.0k
0
votes
2
replies
3.1k
views
Is it possible to multiplex mora than 384 samples on Novaseq 6000 for a very low pass (0.5-10x) WGS?
WGS
Novaseq
5.9 years ago by
Biomed
5.0k
11
votes
0
replies
125k
views
Answer:
A: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
updated 6.2 years ago by
Ram
44k • written 14.3 years ago by
Biomed
5.0k
2
votes
0
replies
125k
views
Comment:
C: Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
updated 6.2 years ago by
Ram
44k • written 14.3 years ago by
Biomed
5.0k
8
votes
4
replies
4.0k
views
Dbsnp Genotypes Confusion
dbsnp
genotyping
updated 6.2 years ago by
Ram
44k • written 14.4 years ago by
Biomed
5.0k
0
votes
3
replies
4.8k
views
Answer:
A: Convert Amos Bank To Ace File
updated 6.2 years ago by
Ram
44k • written 14.3 years ago by
Biomed
5.0k
0
votes
1
reply
2.3k
views
Comment:
C: Is Clinvar the most comprehensive and reliable source of disease-causing genes a
6.3 years ago by
Biomed
5.0k
5
votes
6
replies
2.3k
views
Is Clinvar the most comprehensive and reliable source of disease-causing genes and variants?
clinvar
disease-causing
genetic-disease
omim
6.3 years ago by
Biomed
5.0k
2
votes
1
reply
1.5k
views
Expired Illumina GSA chips
SNP
chip
GSA
6.3 years ago by
Biomed
5.0k
119
votes
25
replies
125k
views
12 follow
Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
human
fasta
sequence
bwa
updated 7.7 years ago by
Hajk-Georg Drost
▴ 170 • written 14.3 years ago by
Biomed
5.0k
12
votes
5
replies
3.0k
views
What Is A Good Computer Science Journal For The Non-Computer Scientist?
updated 7.9 years ago by
Biostar
20 • written 13.8 years ago by
Biomed
5.0k
3
votes
5
replies
2.3k
views
What are the resources to design the most comprehensive clinical SNP chip?
SNP
clinical
primary care
8.4 years ago by
Biomed
5.0k
17
votes
9
replies
14k
views
How Can I Get These Information About Bam Files?
bam
next-gen
sequencing
updated 8.4 years ago by
Biostar
20 • written 13.9 years ago by
Biomed
5.0k
0
votes
0
replies
2.3k
views
Comment:
C: What are the resources to design the most comprehensive clinical SNP chip?
8.4 years ago by
Biomed
5.0k
0
votes
1
reply
2.3k
views
Comment:
C: How can design the most comprehensive "clinical" SNP chip?
8.5 years ago by
Biomed
5.0k
13
votes
7
replies
5.6k
views
Export2Fastq Conversion
fastq
illumina
next-gen
sequencing
updated 8.6 years ago by
ajguerras
• 0 • written 14.3 years ago by
Biomed
5.0k
53
votes
16
replies
36k
views
14 follow
Dbsnp : Best Way To Obtain Data On Snps
dbsnp
updated 2.7 years ago by
Nance
▴ 10 • written 14.4 years ago by
Biomed
5.0k
3
votes
5
replies
4.6k
views
Pysam Snp Calling
updated 9.7 years ago by
Biostar
20 • written 13.4 years ago by
Biomed
5.0k
237
votes
45
replies
73k
views
34 follow
What Is The Best Pipeline For Human Whole Exome Sequencing?
next-gen
sequencing
illumina
exome
human
updated 13.4 years ago by
User 9126
▴ 50 • written 14.4 years ago by
Biomed
5.0k
8
votes
6
replies
5.1k
views
Haplotype Determination With Next-Gen Data In Nuclear Families
haplotype
next-gen
sequencing
updated 2.9 years ago by
Ram
44k • written 13.9 years ago by
Biomed
5.0k
23
votes
12
replies
7.7k
views
7 follow
Dbsnp132 1000Genomes Vcf File Info Field: Bitfield Structure
dbsnp
vcf
genome
updated 10.3 years ago by
cmdcolin
★ 3.9k • written 14.0 years ago by
Biomed
5.0k
20
votes
8
replies
6.2k
views
Baseline Configuration Of A Bioinformatics Server
server
updated 10.7 years ago by
Biostar
20 • written 14.5 years ago by
Biomed
5.0k
11
votes
5
replies
3.8k
views
Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
ucsc
updated 10.8 years ago by
Biostar
20 • written 13.4 years ago by
Biomed
5.0k
50
votes
8
replies
15k
views
9 follow
Expression Databases For Human Genes
gene
updated 11.4 years ago by
Ali R. Vahdati
▴ 190 • written 13.9 years ago by
Biomed
5.0k
39
votes
13
replies
31k
views
10 follow
Human Exome Capture Library Coordinates Download
exome
agilent
next-gen
sequencing
updated 11.4 years ago by
John St. John
★ 1.2k • written 13.8 years ago by
Biomed
5.0k
0
votes
0
replies
4.3k
views
Comment:
C: Conservation At Amino Acid Level
12.3 years ago by
Biomed
5.0k
0
votes
1
reply
4.3k
views
Comment:
C: Conservation At Amino Acid Level
12.4 years ago by
Biomed
5.0k
3
votes
6
replies
4.3k
views
Conservation At Amino Acid Level
conservation
annotation
updated 12.4 years ago by
Leszek
4.2k • written 12.4 years ago by
Biomed
5.0k
2
votes
1
reply
3.0k
views
Functional Validation Of A 5' Utr Mutation
utr
updated 12.4 years ago by
JC
13k • written 12.4 years ago by
Biomed
5.0k
0
votes
0
replies
6.3k
views
Comment:
C: I Need To Plot 73 Mutations On A Large Gene With >60 Exons
12.5 years ago by
Biomed
5.0k
15
votes
6
replies
6.3k
views
I Need To Plot 73 Mutations On A Large Gene With >60 Exons
mutation
gene
plot
updated 12.5 years ago by
Obi Griffith
20k • written 12.5 years ago by
Biomed
5.0k
0
votes
0
replies
5.4k
views
Comment:
C: Which Mappability Track To Use?
12.7 years ago by
Biomed
5.0k
0
votes
0
replies
64k
views
Comment:
C: What Is The Difference Between Hg18 And Hg19?
12.7 years ago by
Biomed
5.0k
0
votes
0
replies
5.4k
views
Comment:
C: Which Mappability Track To Use?
12.7 years ago by
Biomed
5.0k
8
votes
7
replies
5.4k
views
Which Mappability Track To Use?
ucsc
updated 12.7 years ago by
Mikael Huss
4.8k • written 12.7 years ago by
Biomed
5.0k
0
votes
0
replies
64k
views
Comment:
C: What Is The Difference Between Hg18 And Hg19?
12.7 years ago by
Biomed
5.0k
7
votes
6
replies
64k
views
Answer:
A: What Is The Difference Between Hg18 And Hg19?
12.7 years ago by
Biomed
5.0k
5
votes
1
reply
2.8k
views
Why Do We Align Each Pair Set Separately In An Illumina Paired End Sequencing Study?
next-gen
sequencing
updated 12.8 years ago by
Swbarnes2
★ 1.6k • written 12.8 years ago by
Biomed
5.0k
0
votes
0
replies
4.2k
views
Comment:
C: Bwa Aln For Snp/Indel Discovery With Paired End 100Bp Human Dna Reads
12.8 years ago by
Biomed
5.0k
0
votes
0
replies
9.3k
views
Comment:
C: Illlumina Paired End Reads File Format
12.8 years ago by
Biomed
5.0k
6
votes
8
replies
7.2k
views
What Is The Best Program To Determine Structural Variation (Cnv) For Illumina Omniexpress Data?
cnv
illumina
structural
sv
updated 12.8 years ago by
liutao1986
• 0 • written 13.9 years ago by
Biomed
5.0k
23
votes
12
replies
7.5k
views
6 follow
Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Illumina Platform?
illumina
next-gen
sequencing
updated 12.9 years ago by
Larry_Parnell
16k • written 12.9 years ago by
Biomed
5.0k
0
votes
0
replies
7.5k
views
Comment:
C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
12.9 years ago by
Biomed
5.0k
0
votes
0
replies
7.5k
views
Comment:
C: Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Il
12.9 years ago by
Biomed
5.0k
1
vote
1
reply
23k
views
Answer:
A: Converting Illumina Raw Genotype Data Into Plink Ped Format
13.0 years ago by
Biomed
5.0k
166 results • Page
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