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1
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3.3k
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Answer:
Answer: NGS forensics: how to know if data is fabricated
7 months ago by
Prash
▴ 280
0
votes
0
replies
810
views
Answer:
Answer: Why number of interactions decreased in current string database for plasmodium
7 months ago by
Prash
▴ 280
1
vote
0
replies
841
views
Comment:
Comment: Need help understanding core SNPs
8 months ago by
Prash
▴ 280
1
vote
0
replies
1.4k
views
Answer:
Answer: Tower Server configuration for NGS data analysis
10 months ago by
Prash
▴ 280
1
vote
1
reply
991
views
Answer:
Answer: where to work as a bioinformatician (NGS/IA)
updated 10 months ago by
Ram
44k • written 10 months ago by
Prash
▴ 280
0
votes
0
replies
1.3k
views
Answer:
Answer: Mostly Poly-Gs on WGBS sequences.
11 months ago by
Prash
▴ 280
2
votes
1
reply
1.1k
views
Answer:
Answer: LncRNA pipeline
11 months ago by
Prash
▴ 280
2
votes
1
reply
1.1k
views
Answer:
Answer: LncRNA pipeline
11 months ago by
Prash
▴ 280
0
votes
0
replies
1.3k
views
Answer:
Answer: Computing Tajima's D from haploid SNPs
13 months ago by
Prash
▴ 280
0
votes
1
reply
1.5k
views
Answer:
Answer: Somatic CNVs insilico evaluation
16 months ago by
Prash
▴ 280
0
votes
0
replies
2.0k
views
Answer:
Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
16 months ago by
Prash
▴ 280
1
vote
1
reply
1.3k
views
Answer:
Answer: GERP Score for variants
16 months ago by
Prash
▴ 280
0
votes
1
reply
1.5k
views
Answer:
Answer: Somatic CNVs insilico evaluation
17 months ago by
Prash
▴ 280
0
votes
1
reply
1.5k
views
Answer:
Answer: Somatic CNVs insilico evaluation
17 months ago by
Prash
▴ 280
0
votes
0
replies
1.6k
views
Answer:
Answer: Trimming FASTQs
17 months ago by
Prash
▴ 280
0
votes
0
replies
2.2k
views
Comment:
Comment: Why are some WES VCFs larger than others?
18 months ago by
Prash
▴ 280
0
votes
1
reply
2.2k
views
Answer:
Answer: Why are some WES files larger than others?
18 months ago by
Prash
▴ 280
0
votes
0
replies
772
views
Answer:
Answer: Variant calling in WES vs WGS
18 months ago by
Prash
▴ 280
0
votes
0
replies
2.6k
views
Comment:
Comment: Pan genome based assembly
19 months ago by
Prash
▴ 280
0
votes
1
reply
2.6k
views
Answer:
Answer: Pan genome based assembly
19 months ago by
Prash
▴ 280
1
vote
1
reply
2.6k
views
Answer:
Answer: Pan genome based assembly
19 months ago by
Prash
▴ 280
0
votes
0
replies
877
views
Comment:
Comment: How many basepairs are genes padded by in WES?
21 months ago by
Prash
▴ 280
0
votes
1
reply
877
views
Answer:
Answer: How many basepairs are genes padded by in WES?
21 months ago by
Prash
▴ 280
0
votes
0
replies
635
views
Answer:
Answer: interpreting SnpEff output
22 months ago by
Prash
▴ 280
1
vote
0
replies
739
views
Answer:
Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
23 months ago by
Prash
▴ 280
1
vote
0
replies
1.1k
views
Comment:
Comment: Paired - end sequencing
23 months ago by
Prash
▴ 280
1
vote
0
replies
2.3k
views
Answer:
Answer: FASTQC Per base sequence content failed WES
23 months ago by
Prash
▴ 280
0
votes
0
replies
1.0k
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by
Prash
▴ 280
1
vote
1
reply
1.0k
views
Comment:
Comment: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by
Prash
▴ 280
0
votes
1
reply
1.0k
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
2.2 years ago by
Prash
▴ 280
0
votes
1
reply
2.0k
views
Comment:
Comment: NGS Sequence quality
2.2 years ago by
Prash
▴ 280
0
votes
1
reply
2.0k
views
Answer:
Answer: NGS Sequence quality
2.2 years ago by
Prash
▴ 280
0
votes
0
replies
3.1k
views
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
1
vote
1
reply
3.1k
views
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
2
votes
0
replies
1.0k
views
Answer:
Answer: Conceptual questions regarding computational genome/annotation versions and the
2.2 years ago by
Prash
▴ 280
0
votes
0
replies
3.5k
views
Comment:
Comment: Commercial software for genomics / NGS / bioinformatics
2.2 years ago by
Prash
▴ 280
1
vote
1
reply
3.5k
views
Answer:
Answer: Commercial software for genomics / NGS / bioinformatics
2.2 years ago by
Prash
▴ 280
0
votes
0
replies
4.1k
views
Comment:
Comment: How to filter SNPs with excess heterozygosity from a large vcf
2.3 years ago by
Prash
▴ 280
3
votes
1
reply
1.0k
views
Answer:
Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
2.3 years ago by
Prash
▴ 280
0
votes
1
reply
4.1k
views
Answer:
Answer: How to filter SNPs with excess heterozygosity from a large vcf
2.3 years ago by
Prash
▴ 280
1
vote
0
replies
920
views
Answer:
Answer: bioinformatic cost of whole genome sequencing
2.4 years ago by
Prash
▴ 280
1
vote
0
replies
704
views
Answer:
Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
2.6 years ago by
Prash
▴ 280
1
vote
0
replies
891
views
Answer:
Answer: What sequencing method is the most efficient for identifying genes driving rare
2.6 years ago by
Prash
▴ 280
0
votes
0
replies
551
views
Answer:
Answer: How many individuals per SNP?
2.6 years ago by
Prash
▴ 280
0
votes
0
replies
1.9k
views
Comment:
Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
2.6 years ago by
Prash
▴ 280
0
votes
0
replies
722
views
Answer:
Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
2.6 years ago by
Prash
▴ 280
0
votes
0
replies
4.6k
views
Comment:
Comment: Error with per tile sequence quality (by FastQC)
2.6 years ago by
Prash
▴ 280
0
votes
1
reply
4.6k
views
Answer:
Answer: Error with per tile sequence quality (by FastQC)
2.6 years ago by
Prash
▴ 280
0
votes
0
replies
1.1k
views
Comment:
Comment: Variant Allele frequency
2.7 years ago by
Prash
▴ 280
0
votes
1
reply
1.1k
views
Answer:
Answer: Variant Allele frequency
2.7 years ago by
Prash
▴ 280
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