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0
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814
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Answer:
Answer: Somatic CNVs insilico evaluation
7 weeks ago by
Prash
▴ 190
0
votes
0
replies
1.1k
views
Answer:
Answer: Bacteria WGS via illumina short read - is it normal to have 0 coverage in some r
8 weeks ago by
Prash
▴ 190
1
vote
1
reply
588
views
Answer:
Answer: GERP Score for variants
10 weeks ago by
Prash
▴ 190
0
votes
1
reply
814
views
Answer:
Answer: Somatic CNVs insilico evaluation
12 weeks ago by
Prash
▴ 190
0
votes
1
reply
814
views
Answer:
Answer: Somatic CNVs insilico evaluation
12 weeks ago by
Prash
▴ 190
0
votes
0
replies
556
views
Answer:
Answer: Trimming FASTQs
3 months ago by
Prash
▴ 190
0
votes
0
replies
847
views
Comment:
Comment: Why are some WES VCFs larger than others?
4 months ago by
Prash
▴ 190
0
votes
1
reply
847
views
Answer:
Answer: Why are some WES files larger than others?
4 months ago by
Prash
▴ 190
0
votes
0
replies
335
views
Answer:
Answer: Variant calling in WES vs WGS
4 months ago by
Prash
▴ 190
0
votes
0
replies
1.4k
views
Comment:
Comment: Pan genome based assembly
4 months ago by
Prash
▴ 190
0
votes
1
reply
1.4k
views
Answer:
Answer: Pan genome based assembly
4 months ago by
Prash
▴ 190
1
vote
1
reply
1.4k
views
Answer:
Answer: Pan genome based assembly
4 months ago by
Prash
▴ 190
0
votes
0
replies
436
views
Comment:
Comment: How many basepairs are genes padded by in WES?
7 months ago by
Prash
▴ 190
0
votes
1
reply
436
views
Answer:
Answer: How many basepairs are genes padded by in WES?
7 months ago by
Prash
▴ 190
0
votes
0
replies
358
views
Answer:
Answer: interpreting SnpEff output
8 months ago by
Prash
▴ 190
1
vote
0
replies
444
views
Answer:
Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
8 months ago by
Prash
▴ 190
1
vote
0
replies
659
views
Comment:
Comment: Paired - end sequencing
9 months ago by
Prash
▴ 190
1
vote
0
replies
1.2k
views
Answer:
Answer: FASTQC Per base sequence content failed WES
9 months ago by
Prash
▴ 190
0
votes
0
replies
521
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
11 months ago by
Prash
▴ 190
1
vote
1
reply
521
views
Comment:
Comment: Advice on how to generate synthetic Copy Number Variation data
11 months ago by
Prash
▴ 190
0
votes
1
reply
521
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
11 months ago by
Prash
▴ 190
0
votes
1
reply
1.3k
views
Comment:
Comment: NGS Sequence quality
11 months ago by
Prash
▴ 190
0
votes
1
reply
1.3k
views
Answer:
Answer: NGS Sequence quality
11 months ago by
Prash
▴ 190
0
votes
0
replies
1.4k
views
Comment:
Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
12 months ago by
Prash
▴ 190
0
votes
1
reply
1.4k
views
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
2
votes
0
replies
664
views
Answer:
Answer: Conceptual questions regarding computational genome/annotation versions and the
12 months ago by
Prash
▴ 190
0
votes
0
replies
2.0k
views
Comment:
Comment: Commercial software for genomics / NGS / bioinformatics
13 months ago by
Prash
▴ 190
1
vote
1
reply
2.0k
views
Answer:
Answer: Commercial software for genomics / NGS / bioinformatics
13 months ago by
Prash
▴ 190
0
votes
0
replies
2.3k
views
Comment:
Comment: How to filter SNPs with excess heterozygosity from a large vcf
14 months ago by
Prash
▴ 190
3
votes
1
reply
661
views
Answer:
Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
14 months ago by
Prash
▴ 190
0
votes
1
reply
2.3k
views
Answer:
Answer: How to filter SNPs with excess heterozygosity from a large vcf
14 months ago by
Prash
▴ 190
1
vote
0
replies
554
views
Answer:
Answer: bioinformatic cost of whole genome sequencing
14 months ago by
Prash
▴ 190
1
vote
0
replies
426
views
Answer:
Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
17 months ago by
Prash
▴ 190
1
vote
0
replies
627
views
Answer:
Answer: What sequencing method is the most efficient for identifying genes driving rare
17 months ago by
Prash
▴ 190
0
votes
0
replies
322
views
Answer:
Answer: How many individuals per SNP?
17 months ago by
Prash
▴ 190
0
votes
0
replies
1.3k
views
Comment:
Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
17 months ago by
Prash
▴ 190
0
votes
0
replies
469
views
Answer:
Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
18 months ago by
Prash
▴ 190
0
votes
0
replies
1.7k
views
Comment:
Comment: Error with per tile sequence quality (by FastQC)
18 months ago by
Prash
▴ 190
0
votes
1
reply
1.7k
views
Answer:
Answer: Error with per tile sequence quality (by FastQC)
18 months ago by
Prash
▴ 190
0
votes
0
replies
697
views
Comment:
Comment: Variant Allele frequency
18 months ago by
Prash
▴ 190
0
votes
1
reply
697
views
Answer:
Answer: Variant Allele frequency
18 months ago by
Prash
▴ 190
0
votes
0
replies
604
views
Answer:
Answer: Variant calling
18 months ago by
Prash
▴ 190
1
vote
0
replies
463
views
Answer:
Answer: Variant Calling
18 months ago by
Prash
▴ 190
1
vote
0
replies
928
views
Answer:
Answer: SNP downstream analysis
18 months ago by
Prash
▴ 190
0
votes
0
replies
809
views
Comment:
Comment: When to merge BAM or SAM files?
18 months ago by
Prash
▴ 190
0
votes
0
replies
3.5k
views
Answer:
A: 0 mapping hits for blast2go
updated 3.8 years ago by
Ram
40k • written 7.7 years ago by
Prash
▴ 190
0
votes
1
reply
6.4k
views
Answer:
A: Possible Reasons For Intronic Snp Coming Out Top Of Gwas.
updated 3.9 years ago by
Ram
40k • written 8.0 years ago by
Prash
▴ 190
0
votes
0
replies
1.4k
views
Answer:
A: verifyBamID generating error 'VcfFileException'
6.8 years ago by
Prash
▴ 190
0
votes
0
replies
1.7k
views
Answer:
A: How to call SNP's from the consensus file obtained from soapsnp?
7.0 years ago by
Prash
▴ 190
1
vote
1
reply
2.4k
views
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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