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Answer: Answer: NGS forensics: how to know if data is fabricated
3 days ago by Prash ▴ 280
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485
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Answer: Answer: Why number of interactions decreased in current string database for plasmodium
20 days ago by Prash ▴ 280
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0
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551
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Comment: Comment: Need help understanding core SNPs
5 weeks ago by Prash ▴ 280
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0
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818
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Answer: Answer: Tower Server configuration for NGS data analysis
3 months ago by Prash ▴ 280
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740
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Answer: Answer: where to work as a bioinformatician (NGS/IA)
updated 3 months ago by 43k • written 3 months ago by ▴ 280
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833
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Answer: Answer: Mostly Poly-Gs on WGBS sequences.
4 months ago by Prash ▴ 280
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1
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754
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Answer: Answer: LncRNA pipeline
4 months ago by Prash ▴ 280
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1
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754
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Answer: Answer: LncRNA pipeline
4 months ago by Prash ▴ 280
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1.1k
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Answer: Answer: Computing Tajima's D from haploid SNPs
6 months ago by Prash ▴ 280
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1
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1.2k
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Answer: Answer: Somatic CNVs insilico evaluation
8 months ago by Prash ▴ 280
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1.6k
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Answer: Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
9 months ago by Prash ▴ 280
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957
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Answer: Answer: GERP Score for variants
9 months ago by Prash ▴ 280
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1
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1.2k
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Answer: Answer: Somatic CNVs insilico evaluation
9 months ago by Prash ▴ 280
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1
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1.2k
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Answer: Answer: Somatic CNVs insilico evaluation
9 months ago by Prash ▴ 280
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0
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1.1k
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Answer: Answer: Trimming FASTQs
10 months ago by Prash ▴ 280
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0
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1.5k
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Comment: Comment: Why are some WES VCFs larger than others?
11 months ago by Prash ▴ 280
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1
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1.5k
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Answer: Answer: Why are some WES files larger than others?
11 months ago by Prash ▴ 280
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587
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Answer: Answer: Variant calling in WES vs WGS
11 months ago by Prash ▴ 280
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2.0k
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Comment: Comment: Pan genome based assembly
11 months ago by Prash ▴ 280
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1
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2.0k
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Answer: Answer: Pan genome based assembly
11 months ago by Prash ▴ 280
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1
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2.0k
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Answer: Answer: Pan genome based assembly
11 months ago by Prash ▴ 280
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0
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671
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Comment: Comment: How many basepairs are genes padded by in WES?
14 months ago by Prash ▴ 280
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1
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671
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Answer: Answer: How many basepairs are genes padded by in WES?
14 months ago by Prash ▴ 280
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0
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513
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Answer: Answer: interpreting SnpEff output
15 months ago by Prash ▴ 280
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0
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590
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
15 months ago by Prash ▴ 280
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0
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880
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Comment: Comment: Paired - end sequencing
16 months ago by Prash ▴ 280
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0
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1.8k
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Answer: Answer: FASTQC Per base sequence content failed WES
16 months ago by Prash ▴ 280
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0
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762
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
19 months ago by Prash ▴ 280
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762
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
19 months ago by Prash ▴ 280
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1
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762
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
19 months ago by Prash ▴ 280
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1
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1.6k
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Comment: Comment: NGS Sequence quality
19 months ago by Prash ▴ 280
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1
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1.6k
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Answer: Answer: NGS Sequence quality
19 months ago by Prash ▴ 280
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0
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2.3k
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
19 months ago by Prash ▴ 280
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1
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2.3k
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
19 months ago by Prash ▴ 280
2
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0
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831
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
19 months ago by Prash ▴ 280
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0
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2.9k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
20 months ago by Prash ▴ 280
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1
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2.9k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
20 months ago by Prash ▴ 280
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0
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3.1k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
21 months ago by Prash ▴ 280
3
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1
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849
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
21 months ago by Prash ▴ 280
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1
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3.1k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
21 months ago by Prash ▴ 280
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0
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728
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Answer: Answer: bioinformatic cost of whole genome sequencing
21 months ago by Prash ▴ 280
1
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0
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569
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
2.0 years ago by Prash ▴ 280
1
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0
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787
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
2.0 years ago by Prash ▴ 280
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0
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451
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Answer: Answer: How many individuals per SNP?
2.0 years ago by Prash ▴ 280
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1.6k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
2.0 years ago by Prash ▴ 280
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0
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600
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
2.1 years ago by Prash ▴ 280
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0
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2.4k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
2.1 years ago by Prash ▴ 280
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1
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2.4k
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Answer: Answer: Error with per tile sequence quality (by FastQC)
2.1 years ago by Prash ▴ 280
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0
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923
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Comment: Comment: Variant Allele frequency
2.1 years ago by Prash ▴ 280
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1
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923
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Answer: Answer: Variant Allele frequency
2.1 years ago by Prash ▴ 280
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