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Answer: Answer: NGS forensics: how to know if data is fabricated
7 months ago by Prash ▴ 280
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810
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Answer: Answer: Why number of interactions decreased in current string database for plasmodium
7 months ago by Prash ▴ 280
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0
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841
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Comment: Comment: Need help understanding core SNPs
8 months ago by Prash ▴ 280
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1.4k
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Answer: Answer: Tower Server configuration for NGS data analysis
10 months ago by Prash ▴ 280
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991
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Answer: Answer: where to work as a bioinformatician (NGS/IA)
updated 10 months ago by 44k • written 10 months ago by ▴ 280
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1.3k
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Answer: Answer: Mostly Poly-Gs on WGBS sequences.
11 months ago by Prash ▴ 280
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1.1k
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Answer: Answer: LncRNA pipeline
11 months ago by Prash ▴ 280
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1.1k
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Answer: Answer: LncRNA pipeline
11 months ago by Prash ▴ 280
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1.3k
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Answer: Answer: Computing Tajima's D from haploid SNPs
13 months ago by Prash ▴ 280
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1.5k
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Answer: Answer: Somatic CNVs insilico evaluation
16 months ago by Prash ▴ 280
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2.0k
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Answer: Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
16 months ago by Prash ▴ 280
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1.3k
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Answer: Answer: GERP Score for variants
16 months ago by Prash ▴ 280
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1.5k
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Answer: Answer: Somatic CNVs insilico evaluation
17 months ago by Prash ▴ 280
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1.5k
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Answer: Answer: Somatic CNVs insilico evaluation
17 months ago by Prash ▴ 280
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1.6k
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Answer: Answer: Trimming FASTQs
17 months ago by Prash ▴ 280
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2.2k
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Comment: Comment: Why are some WES VCFs larger than others?
18 months ago by Prash ▴ 280
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2.2k
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Answer: Answer: Why are some WES files larger than others?
18 months ago by Prash ▴ 280
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772
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Answer: Answer: Variant calling in WES vs WGS
18 months ago by Prash ▴ 280
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2.6k
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Comment: Comment: Pan genome based assembly
19 months ago by Prash ▴ 280
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2.6k
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Answer: Answer: Pan genome based assembly
19 months ago by Prash ▴ 280
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1
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2.6k
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Answer: Answer: Pan genome based assembly
19 months ago by Prash ▴ 280
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877
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Comment: Comment: How many basepairs are genes padded by in WES?
21 months ago by Prash ▴ 280
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877
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Answer: Answer: How many basepairs are genes padded by in WES?
21 months ago by Prash ▴ 280
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635
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Answer: Answer: interpreting SnpEff output
22 months ago by Prash ▴ 280
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739
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
23 months ago by Prash ▴ 280
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1.1k
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Comment: Comment: Paired - end sequencing
23 months ago by Prash ▴ 280
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0
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2.3k
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Answer: Answer: FASTQC Per base sequence content failed WES
23 months ago by Prash ▴ 280
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1.0k
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by Prash ▴ 280
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1.0k
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by Prash ▴ 280
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1.0k
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by Prash ▴ 280
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1
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2.0k
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Comment: Comment: NGS Sequence quality
2.2 years ago by Prash ▴ 280
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2.0k
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Answer: Answer: NGS Sequence quality
2.2 years ago by Prash ▴ 280
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3.1k
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
2.2 years ago by Prash ▴ 280
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3.1k
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
2.2 years ago by Prash ▴ 280
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1.0k
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
2.2 years ago by Prash ▴ 280
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0
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3.5k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
2.2 years ago by Prash ▴ 280
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1
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3.5k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
2.2 years ago by Prash ▴ 280
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0
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4.1k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
2.3 years ago by Prash ▴ 280
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1.0k
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
2.3 years ago by Prash ▴ 280
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1
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4.1k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
2.3 years ago by Prash ▴ 280
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0
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920
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Answer: Answer: bioinformatic cost of whole genome sequencing
2.4 years ago by Prash ▴ 280
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0
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704
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
2.6 years ago by Prash ▴ 280
1
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0
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891
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
2.6 years ago by Prash ▴ 280
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551
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Answer: Answer: How many individuals per SNP?
2.6 years ago by Prash ▴ 280
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1.9k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
2.6 years ago by Prash ▴ 280
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0
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722
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
2.6 years ago by Prash ▴ 280
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4.6k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
2.6 years ago by Prash ▴ 280
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4.6k
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Answer: Answer: Error with per tile sequence quality (by FastQC)
2.6 years ago by Prash ▴ 280
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0
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1.1k
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Comment: Comment: Variant Allele frequency
2.7 years ago by Prash ▴ 280
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1
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1.1k
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Answer: Answer: Variant Allele frequency
2.7 years ago by Prash ▴ 280
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