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207
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Answer: Answer: interpreting SnpEff output
15 days ago by Prash ▴ 170
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267
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
16 days ago by Prash ▴ 170
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423
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Comment: Comment: Paired - end sequencing
25 days ago by Prash ▴ 170
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617
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Answer: Answer: FASTQC Per base sequence content failed WES
5 weeks ago by Prash ▴ 170
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326
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
3 months ago by Prash ▴ 170
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1
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326
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
3 months ago by Prash ▴ 170
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1
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326
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
3 months ago by Prash ▴ 170
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1
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917
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Comment: Comment: NGS Sequence quality
3 months ago by Prash ▴ 170
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1
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917
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Answer: Answer: NGS Sequence quality
3 months ago by Prash ▴ 170
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476
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
4 months ago by Prash ▴ 170
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1
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476
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
4 months ago by Prash ▴ 170
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0
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471
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
4 months ago by Prash ▴ 170
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1.2k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
4 months ago by Prash ▴ 170
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1
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1.2k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
4 months ago by Prash ▴ 170
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1.3k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
5 months ago by Prash ▴ 170
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488
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
6 months ago by Prash ▴ 170
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1.3k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
6 months ago by Prash ▴ 170
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403
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Answer: Answer: bioinformatic cost of whole genome sequencing
6 months ago by Prash ▴ 170
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279
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
9 months ago by Prash ▴ 170
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0
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437
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
9 months ago by Prash ▴ 170
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227
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Answer: Answer: How many individuals per SNP?
9 months ago by Prash ▴ 170
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765
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
9 months ago by Prash ▴ 170
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349
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
9 months ago by Prash ▴ 170
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0
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907
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Comment: Comment: Error with per tile sequence quality (by FastQC)
9 months ago by Prash ▴ 170
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1
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907
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Answer: Answer: Error with per tile sequence quality (by FastQC)
9 months ago by Prash ▴ 170
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0
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482
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Comment: Comment: Variant Allele frequency
9 months ago by Prash ▴ 170
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1
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482
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Answer: Answer: Variant Allele frequency
9 months ago by Prash ▴ 170
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432
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Answer: Answer: Variant calling
9 months ago by Prash ▴ 170
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0
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331
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Answer: Answer: Variant Calling
10 months ago by Prash ▴ 170
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0
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672
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Answer: Answer: SNP downstream analysis
10 months ago by Prash ▴ 170
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514
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Comment: Comment: When to merge BAM or SAM files?
10 months ago by Prash ▴ 170
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3.2k
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Answer: A: 0 mapping hits for blast2go
updated 3.1 years ago by 37k • written 7.0 years ago by ▴ 170
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1
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6.1k
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Answer: A: Possible Reasons For Intronic Snp Coming Out Top Of Gwas.
updated 3.2 years ago by 37k • written 7.3 years ago by ▴ 170
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1.3k
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Answer: A: verifyBamID generating error 'VcfFileException'
6.1 years ago by Prash ▴ 170
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0
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1.6k
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Answer: A: How to call SNP's from the consensus file obtained from soapsnp?
6.3 years ago by Prash ▴ 170
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1
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2.2k
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Answer: A: Translational bioinformatics in the era of real-time biomedical, health care and
6.9 years ago by Prash ▴ 170
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0
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4.1k
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Answer: A: Getting Protein Information from NCBI Gene ID
updated 7.7 years ago by 37k • written 7.7 years ago by ▴ 170
37 results • Page 1 of 1
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