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6.8k
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Comment: Comment: Human Variation Databases
updated 3.6 years ago by 44k • written 13.2 years ago by 5.0k
5
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5
replies
2.3k
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Assembly For Rare Variants
snp local
updated 13.2 years ago by ★ 3.2k • written 13.2 years ago by 5.0k
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0
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2.3k
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Comment: C: Assembly For Rare Variants
13.2 years ago by Biomed 5.0k
0
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0
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2.3k
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Comment: C: Assembly For Rare Variants
13.2 years ago by Biomed 5.0k
6
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14
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4.2k
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Affy Data Into Illumina Genome Studio
affymetrix illumina
updated 13.3 years ago by 49k • written 14.5 years ago by 5.0k
8
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7
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3.4k
views
Macrogen Vs Complete Genomics
genome sequencing
updated 13.3 years ago by 33k • written 13.5 years ago by 5.0k
7
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1
reply
3.0k
views
What Are The Metrics To Determine The Quality Of A Whole Genome Sequence
genome next-gen sequencing quality
updated 13.3 years ago by ★ 1.9k • written 13.5 years ago by 5.0k
4
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1
reply
3.4k
views
Detecting And Maping Balanced Translocations With Whole Genome Sequencing?
short next-gen sequencing
updated 13.3 years ago by 27k • written 13.5 years ago by 5.0k
1
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2
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5.0k
views
Liftover With Chr_Random Positions
liftover chromosome random
updated 13.3 years ago by 14k • written 13.4 years ago by 5.0k
14
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11
replies
4.9k
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Chr_Random Positions
chromosome random exome sequencing variant
updated 13.3 years ago by ▴ 390 • written 13.6 years ago by 5.0k
10
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9
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4.5k
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How To Predict Which Next Gen Variants Would Not Validate By Sanger
bam samtools exome
updated 13.3 years ago by ▴ 620 • written 13.3 years ago by 5.0k
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0
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4.5k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
13.3 years ago by Biomed 5.0k
0
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0
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4.5k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
13.3 years ago by Biomed 5.0k
6
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8
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5.0k
views
Nextgene As An Alignment And Variant Calling Pipeline
bwa samtools exome
updated 13.4 years ago by 4.2k • written 13.4 years ago by 5.0k
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0
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5.0k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
13.4 years ago by Biomed 5.0k
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0
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5.0k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
13.4 years ago by Biomed 5.0k
15
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4
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5.8k
views
Variant Annotation - Which Transcript(S) Are The Best Representatives Of The Variant?
variant variant annotation genetics
updated 13.4 years ago by 27k • written 13.4 years ago by 5.0k
12
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2
replies
4.2k
views
Is There A Biostar For Biology Questions?
meta biostars
updated 21 months ago by 44k • written 13.4 years ago by 5.0k
0
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0
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3.8k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
13.4 years ago by Biomed 5.0k
0
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0
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3.8k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
13.4 years ago by Biomed 5.0k
8
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2
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6.2k
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What'S Are The Main Differences Between Seattleseq And Annovar?
annovar
updated 13.4 years ago by 14k • written 13.4 years ago by 5.0k
0
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1
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7.0k
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Answer: A: Vcf File For Reference (Exome Sequencing)
13.4 years ago by Biomed 5.0k
0
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0
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4.6k
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Comment: C: Pysam Snp Calling
13.5 years ago by Biomed 5.0k
0
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0
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4.6k
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Comment: C: Pysam Snp Calling
13.5 years ago by Biomed 5.0k
0
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0
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4.6k
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Comment: C: Pysam Snp Calling
13.5 years ago by Biomed 5.0k
0
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0
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3.4k
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Comment: C: Macrogen Vs Complete Genomics
13.5 years ago by Biomed 5.0k
0
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0
replies
3.4k
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Comment: C: Macrogen Vs Complete Genomics
13.5 years ago by Biomed 5.0k
0
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0
replies
4.9k
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Comment: C: Chr_Random Positions
13.6 years ago by Biomed 5.0k
0
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0
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4.9k
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Comment: C: Chr_Random Positions
13.6 years ago by Biomed 5.0k
2
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2
replies
4.5k
views
Answer: Answer: Deep Exome Sequencing And Alignment To Hg18 Or Hg19?
updated 3.6 years ago by 44k • written 13.6 years ago by 5.0k
0
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0
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7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
0
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0
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7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
29
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19
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7.5k
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6 follow
Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
hg hg human
updated 13.6 years ago by ★ 3.6k • written 13.6 years ago by 5.0k
0
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0
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7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
0
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0
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7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
0
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0
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7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
0
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0
replies
7.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
13.6 years ago by Biomed 5.0k
4
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0
replies
4.5k
views
Answer: A: Does Liftover Have Single-Base Resolution?
13.6 years ago by Biomed 5.0k
0
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1
reply
31k
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Comment: C: Human Exome Capture Library Coordinates Download
13.6 years ago by Biomed 5.0k
0
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0
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6.8k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
13.7 years ago by Biomed 5.0k
0
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0
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6.8k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
13.7 years ago by Biomed 5.0k
0
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0
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2.7k
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Comment: C: Non Uniform Gene Coverage And Cufflinks Predictions : Artifacts ?
13.7 years ago by Biomed 5.0k
26
votes
2
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6.1k
views
Multiple Entries With The Same Rs Number In Dbsnp131
snp mapping dbsnp
updated 13.7 years ago by 14k • written 14.2 years ago by 5.0k
1
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3
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3.8k
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Answer: A: Finding Papers About Well-Characterized Snps
13.7 years ago by Biomed 5.0k
10
votes
3
replies
4.4k
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Genomic Change To Aa Change?
variant sequence
updated 23 months ago by 44k • written 13.7 years ago by 5.0k
0
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0
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6.5k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
13.8 years ago by Biomed 5.0k
0
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0
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6.5k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
13.8 years ago by Biomed 5.0k
22
votes
13
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6.5k
views
6 follow
I Need A List Of Bayesian Snp/Genotype Callers
snp genotyping next-gen sequencing
updated 13.8 years ago by ▴ 10 • written 13.8 years ago by 5.0k
0
votes
0
replies
3.2k
views
Comment: C: Snp Position Problem
13.8 years ago by Biomed 5.0k
9
votes
2
replies
3.2k
views
Snp Position Problem
dbsnp position snp genome ucsc
updated 13.8 years ago by ▴ 660 • written 13.8 years ago by 5.0k
166 results • Page 2 of 4
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