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Comment: Comment: Human Variation Databases
updated 2.5 years ago by 40k • written 12.0 years ago by 4.9k
5
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5
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1.9k
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Assembly For Rare Variants
snp local
updated 12.0 years ago by ★ 3.1k • written 12.0 years ago by 4.9k
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0
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1.9k
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Comment: C: Assembly For Rare Variants
12.0 years ago by Biomed 4.9k
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0
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1.9k
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Comment: C: Assembly For Rare Variants
12.0 years ago by Biomed 4.9k
6
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14
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3.6k
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Affy Data Into Illumina Genome Studio
affymetrix illumina
updated 12.1 years ago by 49k • written 13.4 years ago by 4.9k
8
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7
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2.9k
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Macrogen Vs Complete Genomics
genome sequencing
updated 12.1 years ago by 33k • written 12.3 years ago by 4.9k
7
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1
reply
2.8k
views
What Are The Metrics To Determine The Quality Of A Whole Genome Sequence
genome next-gen sequencing quality
updated 12.1 years ago by ★ 1.9k • written 12.3 years ago by 4.9k
4
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1
reply
3.2k
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Detecting And Maping Balanced Translocations With Whole Genome Sequencing?
short next-gen sequencing
updated 12.1 years ago by 26k • written 12.3 years ago by 4.9k
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2
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4.6k
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Liftover With Chr_Random Positions
liftover chromosome random
updated 12.2 years ago by 14k • written 12.3 years ago by 4.9k
14
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11
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4.0k
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Chr_Random Positions
chromosome random exome sequencing variant
updated 12.2 years ago by ▴ 390 • written 12.4 years ago by 4.9k
10
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9
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4.0k
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How To Predict Which Next Gen Variants Would Not Validate By Sanger
bam samtools exome
updated 12.2 years ago by ▴ 620 • written 12.2 years ago by 4.9k
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0
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4.0k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.2 years ago by Biomed 4.9k
0
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0
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4.0k
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Comment: C: How To Predict Which Next Gen Variants Would Not Validate By Sanger
12.2 years ago by Biomed 4.9k
6
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8
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4.5k
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Nextgene As An Alignment And Variant Calling Pipeline
bwa samtools exome
updated 12.3 years ago by 4.2k • written 12.3 years ago by 4.9k
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0
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4.5k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.3 years ago by Biomed 4.9k
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0
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4.5k
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Comment: C: Nextgene As An Alignment And Variant Calling Pipeline
12.3 years ago by Biomed 4.9k
15
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4
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5.3k
views
Variant Annotation - Which Transcript(S) Are The Best Representatives Of The Variant?
variant variant annotation genetics
updated 12.3 years ago by 26k • written 12.3 years ago by 4.9k
12
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2
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4.0k
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Is There A Biostar For Biology Questions?
meta biostars
updated 7 months ago by 40k • written 12.3 years ago by 4.9k
0
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0
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3.4k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.3 years ago by Biomed 4.9k
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0
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3.4k
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Comment: C: Jumping To The Next Bed Coordinate In The Ucsc Genome Browser
12.3 years ago by Biomed 4.9k
8
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2
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5.8k
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What'S Are The Main Differences Between Seattleseq And Annovar?
annovar
updated 12.3 years ago by 14k • written 12.3 years ago by 4.9k
0
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1
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6.4k
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Answer: A: Vcf File For Reference (Exome Sequencing)
12.3 years ago by Biomed 4.9k
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0
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4.1k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
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0
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4.1k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
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0
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4.1k
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Comment: C: Pysam Snp Calling
12.3 years ago by Biomed 4.9k
0
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0
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2.9k
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Comment: C: Macrogen Vs Complete Genomics
12.3 years ago by Biomed 4.9k
0
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0
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2.9k
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Comment: C: Macrogen Vs Complete Genomics
12.3 years ago by Biomed 4.9k
0
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0
replies
4.0k
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Comment: C: Chr_Random Positions
12.4 years ago by Biomed 4.9k
0
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0
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4.0k
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Comment: C: Chr_Random Positions
12.4 years ago by Biomed 4.9k
2
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2
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4.0k
views
Answer: Answer: Deep Exome Sequencing And Alignment To Hg18 Or Hg19?
updated 2.5 years ago by 40k • written 12.4 years ago by 4.9k
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
0
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
29
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19
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6.5k
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6 follow
Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
hg hg human
updated 12.4 years ago by ★ 3.6k • written 12.4 years ago by 4.9k
0
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
0
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
0
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
0
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0
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6.5k
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Comment: C: Reasons For Observing Non-Reference Allele In Everyone As Homozygous Genotype
12.4 years ago by Biomed 4.9k
4
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0
replies
4.1k
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Answer: A: Does Liftover Have Single-Base Resolution?
12.4 years ago by Biomed 4.9k
0
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1
reply
29k
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Comment: C: Human Exome Capture Library Coordinates Download
12.5 years ago by Biomed 4.9k
0
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0
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5.6k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
12.5 years ago by Biomed 4.9k
0
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0
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5.6k
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Comment: C: What Do Bioinformaticians Use To Make High Quality Web Sites?
12.5 years ago by Biomed 4.9k
0
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0
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2.3k
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Comment: C: Non Uniform Gene Coverage And Cufflinks Predictions : Artifacts ?
12.5 years ago by Biomed 4.9k
26
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2
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5.7k
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Multiple Entries With The Same Rs Number In Dbsnp131
snp mapping dbsnp
updated 12.6 years ago by 14k • written 13.1 years ago by 4.9k
1
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3
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3.2k
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Answer: A: Finding Papers About Well-Characterized Snps
12.6 years ago by Biomed 4.9k
10
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3
replies
4.1k
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Genomic Change To Aa Change?
variant sequence
updated 9 months ago by 40k • written 12.6 years ago by 4.9k
0
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0
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5.8k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
12.6 years ago by Biomed 4.9k
0
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0
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5.8k
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Comment: C: I Need A List Of Bayesian Snp/Genotype Callers
12.6 years ago by Biomed 4.9k
22
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13
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5.8k
views
6 follow
I Need A List Of Bayesian Snp/Genotype Callers
snp genotyping next-gen sequencing
updated 12.6 years ago by ▴ 10 • written 12.6 years ago by 4.9k
0
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0
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2.9k
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Comment: C: Snp Position Problem
12.7 years ago by Biomed 4.9k
9
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2
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2.9k
views
Snp Position Problem
dbsnp position snp genome ucsc
updated 12.7 years ago by ▴ 660 • written 12.7 years ago by 4.9k
166 results • Page 2 of 4
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