Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Profile
Posts
Awards
Show
all
questions
tools
blogs
news
tutorials
forum
answers
comments
Showing :
questions
345
votes
94
replies
247k
views
59 follow
Tools To Calculate Average Coverage For A Bam File?
coverage
bam
sequencing
updated 25 days ago by
GenoMax
145k • written 13.6 years ago by
Biomed
5.0k
124
votes
13
replies
178k
views
13 follow
How Can I Convert Bam To Sam?
bam
next-gen-sequencing
sam
updated 12 months ago by
Ram
44k • written 14.1 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 4.7 years ago by
Charles Warden
8.2k • written 12.9 years ago by
Biomed
5.0k
42
votes
6
replies
25k
views
6 follow
Can You Please Tell Me Where I Find Information About .Fai File Format?
maf
gatk
updated 5.1 years ago by
John Marshall
3.1k • written 14.2 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 5.8 years ago by
ATpoint
84k • written 5.8 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
5.8 years ago by
Biomed
5.0k
8
votes
4
replies
3.9k
views
Dbsnp Genotypes Confusion
dbsnp
genotyping
updated 6.0 years ago by
Ram
44k • written 14.2 years ago by
Biomed
5.0k
5
votes
6
replies
2.2k
views
Is Clinvar the most comprehensive and reliable source of disease-causing genes and variants?
clinvar
disease-causing
genetic-disease
omim
6.1 years ago by
Biomed
5.0k
2
votes
1
reply
1.5k
views
Expired Illumina GSA chips
SNP
chip
GSA
6.1 years ago by
Biomed
5.0k
119
votes
25
replies
124k
views
12 follow
Where Can I Download Human Reference Genome In Fasta Format? Hgref.Fa File
human
fasta
sequence
bwa
updated 7.6 years ago by
Hajk-Georg Drost
▴ 160 • written 14.1 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 7.8 years ago by
Biostar
20 • written 13.6 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
8.2 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 8.2 years ago by
Biostar
20 • written 13.7 years ago by
Biomed
5.0k
13
votes
7
replies
5.5k
views
Export2Fastq Conversion
fastq
illumina
next-gen
sequencing
updated 8.4 years ago by
ajguerras
• 0 • written 14.1 years ago by
Biomed
5.0k
53
votes
16
replies
36k
views
14 follow
Dbsnp : Best Way To Obtain Data On Snps
dbsnp
updated 2.5 years ago by
Nance
• 0 • written 14.3 years ago by
Biomed
5.0k
3
votes
5
replies
4.5k
views
Pysam Snp Calling
updated 9.6 years ago by
Biostar
20 • written 13.2 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 13.2 years ago by
User 9126
▴ 50 • written 14.3 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 2.7 years ago by
Ram
44k • written 13.7 years ago by
Biomed
5.0k
23
votes
12
replies
7.6k
views
7 follow
Dbsnp132 1000Genomes Vcf File Info Field: Bitfield Structure
dbsnp
vcf
genome
updated 10.1 years ago by
cmdcolin
★ 3.9k • written 13.8 years ago by
Biomed
5.0k
20
votes
8
replies
6.1k
views
Baseline Configuration Of A Bioinformatics Server
server
updated 10.5 years ago by
Biostar
20 • written 14.3 years ago by
Biomed
5.0k
11
votes
5
replies
3.7k
views
Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
ucsc
updated 10.6 years ago by
Biostar
20 • written 13.2 years ago by
Biomed
5.0k
50
votes
8
replies
15k
views
9 follow
Expression Databases For Human Genes
gene
updated 11.3 years ago by
Ali R. Vahdati
▴ 190 • written 13.8 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 11.3 years ago by
John St. John
★ 1.2k • written 13.6 years ago by
Biomed
5.0k
3
votes
6
replies
4.3k
views
Conservation At Amino Acid Level
conservation
annotation
updated 12.2 years ago by
Leszek
4.2k • written 12.2 years ago by
Biomed
5.0k
2
votes
1
reply
3.0k
views
Functional Validation Of A 5' Utr Mutation
utr
updated 12.2 years ago by
JC
13k • written 12.2 years ago by
Biomed
5.0k
15
votes
6
replies
6.2k
views
I Need To Plot 73 Mutations On A Large Gene With >60 Exons
mutation
gene
plot
updated 12.3 years ago by
Obi Griffith
20k • written 12.3 years ago by
Biomed
5.0k
8
votes
7
replies
5.3k
views
Which Mappability Track To Use?
ucsc
updated 12.6 years ago by
Mikael Huss
4.8k • written 12.6 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 12.6 years ago by
Swbarnes2
★ 1.6k • written 12.6 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 12.6 years ago by
liutao1986
• 0 • written 13.7 years ago by
Biomed
5.0k
23
votes
12
replies
7.4k
views
6 follow
Reasons Why A Region In The Human Genome May Get Bad Sequence/Alignment Using Illumina Platform?
illumina
next-gen
sequencing
updated 12.7 years ago by
Larry_Parnell
16k • written 12.7 years ago by
Biomed
5.0k
5
votes
5
replies
2.2k
views
Assembly For Rare Variants
snp
local
updated 13.0 years ago by
Lee Katz
★ 3.2k • written 13.0 years ago by
Biomed
5.0k
6
votes
14
replies
4.1k
views
Affy Data Into Illumina Genome Studio
affymetrix
illumina
updated 13.0 years ago by
Neilfws
49k • written 14.3 years ago by
Biomed
5.0k
8
votes
7
replies
3.4k
views
Macrogen Vs Complete Genomics
genome
sequencing
updated 13.0 years ago by
lh3
33k • written 13.3 years ago by
Biomed
5.0k
7
votes
1
reply
2.9k
views
What Are The Metrics To Determine The Quality Of A Whole Genome Sequence
genome
next-gen
sequencing
quality
updated 13.0 years ago by
Pablo
★ 1.9k • written 13.3 years ago by
Biomed
5.0k
4
votes
1
reply
3.4k
views
Detecting And Maping Balanced Translocations With Whole Genome Sequencing?
short
next-gen
sequencing
updated 13.0 years ago by
Sean Davis
27k • written 13.2 years ago by
Biomed
5.0k
1
vote
2
replies
4.9k
views
Liftover With Chr_Random Positions
liftover
chromosome
random
updated 13.1 years ago by
Jorge Amigo
14k • written 13.2 years ago by
Biomed
5.0k
14
votes
11
replies
4.7k
views
Chr_Random Positions
chromosome
random
exome
sequencing
variant
updated 13.1 years ago by
Ning-Yi Shao
▴ 390 • written 13.3 years ago by
Biomed
5.0k
10
votes
9
replies
4.4k
views
How To Predict Which Next Gen Variants Would Not Validate By Sanger
bam
samtools
exome
updated 13.1 years ago by
Bioinfosm
▴ 620 • written 13.1 years ago by
Biomed
5.0k
6
votes
8
replies
4.9k
views
Nextgene As An Alignment And Variant Calling Pipeline
bwa
samtools
exome
updated 13.2 years ago by
Leszek
4.2k • written 13.2 years ago by
Biomed
5.0k
15
votes
4
replies
5.7k
views
Variant Annotation - Which Transcript(S) Are The Best Representatives Of The Variant?
variant
variant
annotation
genetics
updated 13.2 years ago by
Sean Davis
27k • written 13.2 years ago by
Biomed
5.0k
12
votes
2
replies
4.2k
views
Is There A Biostar For Biology Questions?
meta
biostars
updated 18 months ago by
Ram
44k • written 13.2 years ago by
Biomed
5.0k
8
votes
2
replies
6.1k
views
What'S Are The Main Differences Between Seattleseq And Annovar?
annovar
updated 13.2 years ago by
Jorge Amigo
14k • written 13.2 years ago by
Biomed
5.0k
29
votes
19
replies
7.3k
views
6 follow
Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
hg
hg
human
updated 13.4 years ago by
Ryan Thompson
★ 3.6k • written 13.4 years ago by
Biomed
5.0k
26
votes
2
replies
6.0k
views
Multiple Entries With The Same Rs Number In Dbsnp131
snp
mapping
dbsnp
updated 13.5 years ago by
Jorge Amigo
14k • written 14.0 years ago by
Biomed
5.0k
10
votes
3
replies
4.4k
views
Genomic Change To Aa Change?
variant
sequence
updated 21 months ago by
Ram
44k • written 13.5 years ago by
Biomed
5.0k
22
votes
13
replies
6.4k
views
6 follow
I Need A List Of Bayesian Snp/Genotype Callers
snp
genotyping
next-gen
sequencing
updated 13.6 years ago by
bgulko2
▴ 10 • written 13.6 years ago by
Biomed
5.0k
9
votes
2
replies
3.1k
views
Snp Position Problem
dbsnp
position
snp
genome
ucsc
updated 13.6 years ago by
Mitch Skinner
▴ 660 • written 13.6 years ago by
Biomed
5.0k
13
votes
6
replies
4.0k
views
Navigating Public Data For A Variant / Variant Annotation
variant
annotation
updated 13.6 years ago by
Brad Chapman
9.7k • written 13.6 years ago by
Biomed
5.0k
13
votes
8
replies
8.5k
views
7 follow
Linkage With Whole Exome Data
exome
linkage
updated 13.6 years ago by
glyamamoto
• 0 • written 14.2 years ago by
Biomed
5.0k
11
votes
4
replies
3.2k
views
Ucsc Dbsnp131 Table Format
dbsnp
bed
ucsc
updated 13.6 years ago by
Stephane Plaisance
▴ 460 • written 14.0 years ago by
Biomed
5.0k
56 results • Page
1 of 2
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6