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565
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Comment: Comment: Why are some WES VCFs larger than others?
12 days ago by Prash ▴ 180
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565
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Answer: Answer: Why are some WES files larger than others?
13 days ago by Prash ▴ 180
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215
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Answer: Answer: Variant calling in WES vs WGS
14 days ago by Prash ▴ 180
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965
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Comment: Comment: Pan genome based assembly
28 days ago by Prash ▴ 180
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965
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Answer: Answer: Pan genome based assembly
28 days ago by Prash ▴ 180
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1
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965
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Answer: Answer: Pan genome based assembly
4 weeks ago by Prash ▴ 180
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318
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Comment: Comment: How many basepairs are genes padded by in WES?
3 months ago by Prash ▴ 180
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318
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Answer: Answer: How many basepairs are genes padded by in WES?
3 months ago by Prash ▴ 180
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0
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287
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Answer: Answer: interpreting SnpEff output
4 months ago by Prash ▴ 180
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361
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
4 months ago by Prash ▴ 180
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0
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545
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Comment: Comment: Paired - end sequencing
5 months ago by Prash ▴ 180
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0
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908
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Answer: Answer: FASTQC Per base sequence content failed WES
5 months ago by Prash ▴ 180
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406
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
8 months ago by Prash ▴ 180
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406
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
8 months ago by Prash ▴ 180
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406
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
8 months ago by Prash ▴ 180
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1
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1.1k
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Comment: Comment: NGS Sequence quality
8 months ago by Prash ▴ 180
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1
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1.1k
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Answer: Answer: NGS Sequence quality
8 months ago by Prash ▴ 180
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0
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929
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
8 months ago by Prash ▴ 180
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1
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929
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
8 months ago by Prash ▴ 180
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0
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567
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
8 months ago by Prash ▴ 180
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0
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1.6k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
9 months ago by Prash ▴ 180
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1
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1.6k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
9 months ago by Prash ▴ 180
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0
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1.8k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
10 months ago by Prash ▴ 180
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1
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567
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
10 months ago by Prash ▴ 180
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1.8k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
10 months ago by Prash ▴ 180
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464
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Answer: Answer: bioinformatic cost of whole genome sequencing
10 months ago by Prash ▴ 180
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0
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342
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
13 months ago by Prash ▴ 180
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0
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528
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
13 months ago by Prash ▴ 180
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264
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Answer: Answer: How many individuals per SNP?
13 months ago by Prash ▴ 180
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1.1k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
14 months ago by Prash ▴ 180
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0
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401
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
14 months ago by Prash ▴ 180
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0
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1.3k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
14 months ago by Prash ▴ 180
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1
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1.3k
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Answer: Answer: Error with per tile sequence quality (by FastQC)
14 months ago by Prash ▴ 180
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0
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602
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Comment: Comment: Variant Allele frequency
14 months ago by Prash ▴ 180
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1
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602
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Answer: Answer: Variant Allele frequency
14 months ago by Prash ▴ 180
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0
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507
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Answer: Answer: Variant calling
14 months ago by Prash ▴ 180
1
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0
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391
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Answer: Answer: Variant Calling
14 months ago by Prash ▴ 180
1
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0
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806
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Answer: Answer: SNP downstream analysis
14 months ago by Prash ▴ 180
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0
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623
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Comment: Comment: When to merge BAM or SAM files?
14 months ago by Prash ▴ 180
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0
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3.3k
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Answer: A: 0 mapping hits for blast2go
updated 3.4 years ago by 39k • written 7.4 years ago by ▴ 180
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6.2k
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Answer: A: Possible Reasons For Intronic Snp Coming Out Top Of Gwas.
updated 3.6 years ago by 39k • written 7.7 years ago by ▴ 180
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0
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1.3k
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Answer: A: verifyBamID generating error 'VcfFileException'
6.5 years ago by Prash ▴ 180
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0
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1.7k
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Answer: A: How to call SNP's from the consensus file obtained from soapsnp?
6.6 years ago by Prash ▴ 180
1
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1
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2.3k
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Answer: A: Translational bioinformatics in the era of real-time biomedical, health care and
7.3 years ago by Prash ▴ 180
1
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0
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4.2k
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Answer: Answer: Getting Protein Information from NCBI Gene ID
updated 4 months ago by 39k • written 8.1 years ago by ▴ 180
45 results • Page 1 of 1
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