Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
0
votes
0
replies
6.4k
views
Comment: Comment: Human Variation Databases
updated 3.1 years ago by 43k • written 12.6 years ago by 5.0k
5
votes
5
replies
2.1k
views
Assembly For Rare Variants
snp local
updated 12.6 years ago by ★ 3.1k • written 12.6 years ago by 5.0k
0
votes
0
replies
2.1k
views
Comment: C: Assembly For Rare Variants
12.6 years ago by Biomed 5.0k
0
votes
0
replies
2.1k
views
Comment: C: Assembly For Rare Variants
12.6 years ago by Biomed 5.0k
6
votes
14
replies
3.9k
views
Affy Data Into Illumina Genome Studio
affymetrix illumina
updated 12.7 years ago by 49k • written 13.9 years ago by 5.0k
8
votes
7
replies
3.2k
views
Macrogen Vs Complete Genomics
genome sequencing
updated 12.7 years ago by 33k • written 12.9 years ago by 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 12.7 years ago by ★ 1.9k • written 12.9 years ago by 5.0k
4
votes
1
reply
3.3k
views
Detecting And Maping Balanced Translocations With Whole Genome Sequencing?
short next-gen sequencing
updated 12.7 years ago by 26k • written 12.9 years ago by 5.0k
1
vote
2
replies
4.7k
views
Liftover With Chr_Random Positions
liftover chromosome random
updated 12.8 years ago by 14k • written 12.9 years ago by 5.0k
14
votes
11
replies
4.4k
views
Chr_Random Positions
chromosome random exome sequencing variant
updated 12.8 years ago by ▴ 390 • written 13.0 years ago by 5.0k
10
votes
9
replies
4.2k
views
How To Predict Which Next Gen Variants Would Not Validate By Sanger
bam samtools exome
updated 12.8 years ago by ▴ 620 • written 12.8 years ago by 5.0k
0
votes
0
replies
4.2k
views
Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.8 years ago by Biomed 5.0k
0
votes
0
replies
4.2k
views
Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.8 years ago by Biomed 5.0k
6
votes
8
replies
4.7k
views
Nextgene As An Alignment And Variant Calling Pipeline
bwa samtools exome
updated 12.8 years ago by 4.2k • written 12.8 years ago by 5.0k
0
votes
0
replies
4.7k
views
Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.8 years ago by Biomed 5.0k
0
votes
0
replies
4.7k
views
Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.8 years ago by Biomed 5.0k
15
votes
4
replies
5.6k
views
Variant Annotation - Which Transcript(S) Are The Best Representatives Of The Variant?
variant variant annotation genetics
updated 12.9 years ago by 26k • written 12.9 years ago by 5.0k
12
votes
2
replies
4.1k
views
Is There A Biostar For Biology Questions?
meta biostars
updated 14 months ago by 43k • written 12.9 years ago by 5.0k
0
votes
0
replies
3.6k
views
Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.9 years ago by Biomed 5.0k
0
votes
0
replies
3.6k
views
Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.9 years ago by Biomed 5.0k
8
votes
2
replies
6.0k
views
What'S Are The Main Differences Between Seattleseq And Annovar?
annovar
updated 12.9 years ago by 14k • written 12.9 years ago by 5.0k
0
votes
1
reply
6.7k
views
Answer: A: Vcf File For Reference (Exome Sequencing)
12.9 years ago by Biomed 5.0k
0
votes
0
replies
4.4k
views
Comment: C: Pysam Snp Calling
12.9 years ago by Biomed 5.0k
0
votes
0
replies
4.4k
views
Comment: C: Pysam Snp Calling
12.9 years ago by Biomed 5.0k
0
votes
0
replies
4.4k
views
Comment: C: Pysam Snp Calling
12.9 years ago by Biomed 5.0k
0
votes
0
replies
3.2k
views
Comment: C: Macrogen Vs Complete Genomics
12.9 years ago by Biomed 5.0k
0
votes
0
replies
3.2k
views
Comment: C: Macrogen Vs Complete Genomics
12.9 years ago by Biomed 5.0k
0
votes
0
replies
4.4k
views
Comment: C: Chr_Random Positions
13.0 years ago by Biomed 5.0k
0
votes
0
replies
4.4k
views
Comment: C: Chr_Random Positions
13.0 years ago by Biomed 5.0k
2
votes
2
replies
4.3k
views
Answer: Answer: Deep Exome Sequencing And Alignment To Hg18 Or Hg19?
updated 3.1 years ago by 43k • written 13.0 years ago by 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
29
votes
19
replies
7.0k
views
6 follow
Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
hg hg human
updated 13.0 years ago by ★ 3.6k • written 13.0 years ago by 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
0
votes
0
replies
7.0k
views
Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.0 years ago by Biomed 5.0k
4
votes
0
replies
4.3k
views
Answer: A: Does Liftover Have Single-Base Resolution?
13.0 years ago by Biomed 5.0k
0
votes
1
reply
30k
views
Comment: C: Human Exome Capture Library Coordinates Download
13.0 years ago by Biomed 5.0k
0
votes
0
replies
6.2k
views
Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
13.1 years ago by Biomed 5.0k
0
votes
0
replies
6.2k
views
Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
13.1 years ago by Biomed 5.0k
0
votes
0
replies
2.5k
views
Comment: C: Non Uniform Gene Coverage And Cufflinks Predictions : Artifacts ?
13.1 years ago by Biomed 5.0k
26
votes
2
replies
5.9k
views
Multiple Entries With The Same Rs Number In Dbsnp131
snp mapping dbsnp
updated 13.1 years ago by 14k • written 13.7 years ago by 5.0k
1
vote
3
replies
3.5k
views
Answer: A: Finding Papers About Well-Characterized Snps
13.2 years ago by Biomed 5.0k
10
votes
3
replies
4.2k
views
Genomic Change To Aa Change?
variant sequence
updated 17 months ago by 43k • written 13.2 years ago by 5.0k
0
votes
0
replies
6.2k
views
Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
13.2 years ago by Biomed 5.0k
0
votes
0
replies
6.2k
views
Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
13.2 years ago by Biomed 5.0k
22
votes
13
replies
6.2k
views
6 follow
I Need A List Of Bayesian Snp/Genotype Callers
snp genotyping next-gen sequencing
updated 13.2 years ago by ▴ 10 • written 13.2 years ago by 5.0k
0
votes
0
replies
3.0k
views
Comment: C: Snp Position Problem
13.2 years ago by Biomed 5.0k
9
votes
2
replies
3.0k
views
Snp Position Problem
dbsnp position snp genome ucsc
updated 13.2 years ago by ▴ 660 • written 13.2 years ago by 5.0k
166 results • Page 2 of 4
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