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Answer: Answer: ACMG assignment tools
5 weeks ago by Prash ▴ 290
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1
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667
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Answer: Answer: Seeking Help for Reanalysis of Raw WES Data
4 months ago by Prash ▴ 290
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463
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Answer: Answer: Low quality of NGS SNP analysis panel
4 months ago by Prash ▴ 290
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5.6k
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Answer: Answer: NGS forensics: how to know if data is fabricated
14 months ago by Prash ▴ 290
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1.4k
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Answer: Answer: Why number of interactions decreased in current string database for plasmodium
15 months ago by Prash ▴ 290
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1.3k
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Comment: Comment: Need help understanding core SNPs
15 months ago by Prash ▴ 290
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2.3k
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Answer: Answer: Tower Server configuration for NGS data analysis
17 months ago by Prash ▴ 290
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1.5k
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Answer: Answer: where to work as a bioinformatician (NGS/IA)
updated 18 months ago by 45k • written 18 months ago by ▴ 290
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1.9k
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Answer: Answer: Mostly Poly-Gs on WGBS sequences.
18 months ago by Prash ▴ 290
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1.5k
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Answer: Answer: LncRNA pipeline
18 months ago by Prash ▴ 290
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1
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1.5k
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Answer: Answer: LncRNA pipeline
19 months ago by Prash ▴ 290
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1.7k
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Answer: Answer: Computing Tajima's D from haploid SNPs
21 months ago by Prash ▴ 290
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1
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2.0k
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Answer: Answer: Somatic CNVs insilico evaluation
23 months ago by Prash ▴ 290
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2.8k
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Answer: Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
23 months ago by Prash ▴ 290
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2
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2.1k
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Answer: Answer: GERP Score for variants
24 months ago by Prash ▴ 290
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1
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2.0k
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Answer: Answer: Somatic CNVs insilico evaluation
2.0 years ago by Prash ▴ 290
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1
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2.0k
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Answer: Answer: Somatic CNVs insilico evaluation
2.0 years ago by Prash ▴ 290
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2.4k
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Answer: Answer: Trimming FASTQs
2.1 years ago by Prash ▴ 290
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3.0k
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Comment: Comment: Why are some WES VCFs larger than others?
2.1 years ago by Prash ▴ 290
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3.0k
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Answer: Answer: Why are some WES files larger than others?
2.1 years ago by Prash ▴ 290
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1.1k
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Answer: Answer: Variant calling in WES vs WGS
2.1 years ago by Prash ▴ 290
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3.8k
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Comment: Comment: Pan genome based assembly
2.2 years ago by Prash ▴ 290
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1
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3.8k
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Answer: Answer: Pan genome based assembly
2.2 years ago by Prash ▴ 290
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1
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3.8k
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Answer: Answer: Pan genome based assembly
2.2 years ago by Prash ▴ 290
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1.3k
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Comment: Comment: How many basepairs are genes padded by in WES?
2.4 years ago by Prash ▴ 290
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1.3k
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Answer: Answer: How many basepairs are genes padded by in WES?
2.4 years ago by Prash ▴ 290
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0
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910
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Answer: Answer: interpreting SnpEff output
2.5 years ago by Prash ▴ 290
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1.0k
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Answer: Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
2.5 years ago by Prash ▴ 290
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1.6k
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Comment: Comment: Paired - end sequencing
2.5 years ago by Prash ▴ 290
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3.0k
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Answer: Answer: FASTQC Per base sequence content failed WES
2.6 years ago by Prash ▴ 290
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0
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1.5k
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
2.8 years ago by Prash ▴ 290
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1
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1.5k
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Comment: Comment: Advice on how to generate synthetic Copy Number Variation data
2.8 years ago by Prash ▴ 290
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1
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1.5k
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Answer: Answer: Advice on how to generate synthetic Copy Number Variation data
2.8 years ago by Prash ▴ 290
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1
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2.5k
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Comment: Comment: NGS Sequence quality
2.8 years ago by Prash ▴ 290
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2.5k
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Answer: Answer: NGS Sequence quality
2.8 years ago by Prash ▴ 290
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4.2k
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Comment: Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
2.8 years ago by Prash ▴ 290
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1
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4.2k
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Answer: Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
2.8 years ago by Prash ▴ 290
2
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0
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1.4k
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Answer: Answer: Conceptual questions regarding computational genome/annotation versions and the
2.8 years ago by Prash ▴ 290
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0
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4.9k
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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
2.8 years ago by Prash ▴ 290
1
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1
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4.9k
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Answer: Answer: Commercial software for genomics / NGS / bioinformatics
2.8 years ago by Prash ▴ 290
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0
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5.1k
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Comment: Comment: How to filter SNPs with excess heterozygosity from a large vcf
2.9 years ago by Prash ▴ 290
3
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1
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1.3k
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Answer: Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
2.9 years ago by Prash ▴ 290
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1
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5.1k
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Answer: Answer: How to filter SNPs with excess heterozygosity from a large vcf
3.0 years ago by Prash ▴ 290
1
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0
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1.4k
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Answer: Answer: bioinformatic cost of whole genome sequencing
3.0 years ago by Prash ▴ 290
1
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0
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939
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Answer: Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
3.2 years ago by Prash ▴ 290
1
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0
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1.1k
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Answer: Answer: What sequencing method is the most efficient for identifying genes driving rare
3.2 years ago by Prash ▴ 290
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0
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784
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Answer: Answer: How many individuals per SNP?
3.2 years ago by Prash ▴ 290
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0
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2.4k
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Comment: Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
3.2 years ago by Prash ▴ 290
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0
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992
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Answer: Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
3.3 years ago by Prash ▴ 290
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0
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7.7k
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Comment: Comment: Error with per tile sequence quality (by FastQC)
3.3 years ago by Prash ▴ 290
63 results • Page 1 of 2
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