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Answer: Answer: Somatic CNVs insilico evaluation
7 weeks ago by Prash ▴ 190
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1.1k
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Answer: Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
8 weeks ago by Prash ▴ 190
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587
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Answer: Answer: GERP Score for variants
10 weeks ago by Prash ▴ 190
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810
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Answer: Answer: Somatic CNVs insilico evaluation
11 weeks ago by Prash ▴ 190
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1
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810
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Answer: Answer: Somatic CNVs insilico evaluation
12 weeks ago by Prash ▴ 190
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552
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Answer: Answer: Trimming FASTQs
3 months ago by Prash ▴ 190
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839
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Answer: Answer: Why are some WES files larger than others?
4 months ago by Prash ▴ 190
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333
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Answer: Answer: Variant calling in WES vs WGS
4 months ago by Prash ▴ 190
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1.4k
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Answer: Answer: Pan genome based assembly
4 months ago by Prash ▴ 190
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1.4k
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Answer: Answer: Pan genome based assembly
4 months ago by Prash ▴ 190
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434
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Answer: Answer: How many basepairs are genes padded by in WES?
7 months ago by Prash ▴ 190
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358
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Answer: Answer: interpreting SnpEff output
8 months ago by Prash ▴ 190
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442
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
8 months ago by Prash ▴ 190
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1.2k
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Answer: Answer: FASTQC Per base sequence content failed WES
9 months ago by Prash ▴ 190
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518
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
11 months ago by Prash ▴ 190
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518
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
11 months ago by Prash ▴ 190
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1.3k
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Answer: Answer: NGS Sequence quality
11 months ago by Prash ▴ 190
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1.4k
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
12 months ago by Prash ▴ 190
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663
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
12 months ago by Prash ▴ 190
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2.0k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
13 months ago by Prash ▴ 190
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659
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
14 months ago by Prash ▴ 190
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2.3k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
14 months ago by Prash ▴ 190
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552
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Answer: Answer: bioinformatic cost of whole genome sequencing
14 months ago by Prash ▴ 190
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421
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
17 months ago by Prash ▴ 190
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627
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
17 months ago by Prash ▴ 190
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320
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Answer: Answer: How many individuals per SNP?
17 months ago by Prash ▴ 190
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468
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
17 months ago by Prash ▴ 190
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1.6k
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Answer: Answer: Error with per tile sequence quality (by FastQC)
17 months ago by Prash ▴ 190
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1
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695
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Answer: Answer: Variant Allele frequency
18 months ago by Prash ▴ 190
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600
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Answer: Answer: Variant calling
18 months ago by Prash ▴ 190
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460
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Answer: Answer: Variant Calling
18 months ago by Prash ▴ 190
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924
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Answer: Answer: SNP downstream analysis
18 months ago by Prash ▴ 190
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3.5k
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Answer: A: 0 mapping hits for blast2go
updated 3.8 years ago by 40k • written 7.7 years ago by ▴ 190
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6.4k
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Answer: A: Possible Reasons For Intronic Snp Coming Out Top Of Gwas.
updated 3.9 years ago by 40k • written 8.0 years ago by ▴ 190
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1.4k
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Answer: A: verifyBamID generating error 'VcfFileException'
6.8 years ago by Prash ▴ 190
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1.7k
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Answer: A: How to call SNP's from the consensus file obtained from soapsnp?
6.9 years ago by Prash ▴ 190
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1
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2.4k
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Answer: A: Translational bioinformatics in the era of real-time biomedical, health care and
7.6 years ago by Prash ▴ 190
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0
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4.3k
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Answer: Answer: Getting Protein Information from NCBI Gene ID
updated 7 months ago by 40k • written 8.4 years ago by ▴ 190
38 results • Page 1 of 1
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