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0
votes
0
replies
565
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Comment:
Comment: Why are some WES VCFs larger than others?
12 days ago by
Prash
▴ 180
0
votes
1
reply
565
views
Answer:
Answer: Why are some WES files larger than others?
13 days ago by
Prash
▴ 180
0
votes
0
replies
215
views
Answer:
Answer: Variant calling in WES vs WGS
14 days ago by
Prash
▴ 180
0
votes
0
replies
965
views
Comment:
Comment: Pan genome based assembly
28 days ago by
Prash
▴ 180
0
votes
1
reply
965
views
Answer:
Answer: Pan genome based assembly
28 days ago by
Prash
▴ 180
1
vote
1
reply
965
views
Answer:
Answer: Pan genome based assembly
4 weeks ago by
Prash
▴ 180
0
votes
0
replies
318
views
Comment:
Comment: How many basepairs are genes padded by in WES?
3 months ago by
Prash
▴ 180
0
votes
1
reply
318
views
Answer:
Answer: How many basepairs are genes padded by in WES?
3 months ago by
Prash
▴ 180
0
votes
0
replies
287
views
Answer:
Answer: interpreting SnpEff output
4 months ago by
Prash
▴ 180
1
vote
0
replies
361
views
Answer:
Answer: Conflicting sequences between Genome Browser and NCBI (reference hg19).
4 months ago by
Prash
▴ 180
1
vote
0
replies
545
views
Comment:
Comment: Paired - end sequencing
5 months ago by
Prash
▴ 180
1
vote
0
replies
908
views
Answer:
Answer: FASTQC Per base sequence content failed WES
5 months ago by
Prash
▴ 180
0
votes
0
replies
406
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
8 months ago by
Prash
▴ 180
1
vote
1
reply
406
views
Comment:
Comment: Advice on how to generate synthetic Copy Number Variation data
8 months ago by
Prash
▴ 180
0
votes
1
reply
406
views
Answer:
Answer: Advice on how to generate synthetic Copy Number Variation data
8 months ago by
Prash
▴ 180
0
votes
1
reply
1.1k
views
Comment:
Comment: NGS Sequence quality
8 months ago by
Prash
▴ 180
0
votes
1
reply
1.1k
views
Answer:
Answer: NGS Sequence quality
8 months ago by
Prash
▴ 180
0
votes
0
replies
929
views
Comment:
Comment: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
8 months ago by
Prash
▴ 180
0
votes
1
reply
929
views
Answer:
Answer: What are R1, R2, R3, and I1 in a illumina sequencing data, and how can I get mor
8 months ago by
Prash
▴ 180
2
votes
0
replies
567
views
Answer:
Answer: Conceptual questions regarding computational genome/annotation versions and the
8 months ago by
Prash
▴ 180
0
votes
0
replies
1.6k
views
Comment:
Comment: Commercial software for genomics / NGS / bioinformatics
9 months ago by
Prash
▴ 180
1
vote
1
reply
1.6k
views
Answer:
Answer: Commercial software for genomics / NGS / bioinformatics
9 months ago by
Prash
▴ 180
0
votes
0
replies
1.8k
views
Comment:
Comment: How to filter SNPs with excess heterozygosity from a large vcf
10 months ago by
Prash
▴ 180
3
votes
1
reply
567
views
Answer:
Answer: Pros and Cons of DNA Mass Spectrometry versus WES/WGS?
10 months ago by
Prash
▴ 180
0
votes
1
reply
1.8k
views
Answer:
Answer: How to filter SNPs with excess heterozygosity from a large vcf
10 months ago by
Prash
▴ 180
1
vote
0
replies
464
views
Answer:
Answer: bioinformatic cost of whole genome sequencing
10 months ago by
Prash
▴ 180
1
vote
0
replies
342
views
Answer:
Answer: Detection of single nucleotide insertion within a tandem repeat region of variab
13 months ago by
Prash
▴ 180
1
vote
0
replies
528
views
Answer:
Answer: What sequencing method is the most efficient for identifying genes driving rare
13 months ago by
Prash
▴ 180
0
votes
0
replies
264
views
Answer:
Answer: How many individuals per SNP?
13 months ago by
Prash
▴ 180
0
votes
0
replies
1.1k
views
Comment:
Comment: WES data analysis: the rationale behind merging BAM files and marking duplicates
14 months ago by
Prash
▴ 180
0
votes
0
replies
401
views
Answer:
Answer: Identify reads that protein-coding and non coding (lncRNAs) for analysis long no
14 months ago by
Prash
▴ 180
0
votes
0
replies
1.3k
views
Comment:
Comment: Error with per tile sequence quality (by FastQC)
14 months ago by
Prash
▴ 180
0
votes
1
reply
1.3k
views
Answer:
Answer: Error with per tile sequence quality (by FastQC)
14 months ago by
Prash
▴ 180
0
votes
0
replies
602
views
Comment:
Comment: Variant Allele frequency
14 months ago by
Prash
▴ 180
0
votes
1
reply
602
views
Answer:
Answer: Variant Allele frequency
14 months ago by
Prash
▴ 180
0
votes
0
replies
507
views
Answer:
Answer: Variant calling
14 months ago by
Prash
▴ 180
1
vote
0
replies
391
views
Answer:
Answer: Variant Calling
14 months ago by
Prash
▴ 180
1
vote
0
replies
806
views
Answer:
Answer: SNP downstream analysis
14 months ago by
Prash
▴ 180
0
votes
0
replies
623
views
Comment:
Comment: When to merge BAM or SAM files?
14 months ago by
Prash
▴ 180
0
votes
0
replies
3.3k
views
Answer:
A: 0 mapping hits for blast2go
updated 3.4 years ago by
Ram
39k • written 7.4 years ago by
Prash
▴ 180
0
votes
1
reply
6.2k
views
Answer:
A: Possible Reasons For Intronic Snp Coming Out Top Of Gwas.
updated 3.6 years ago by
Ram
39k • written 7.7 years ago by
Prash
▴ 180
0
votes
0
replies
1.3k
views
Answer:
A: verifyBamID generating error 'VcfFileException'
6.5 years ago by
Prash
▴ 180
0
votes
0
replies
1.7k
views
Answer:
A: How to call SNP's from the consensus file obtained from soapsnp?
6.6 years ago by
Prash
▴ 180
1
vote
1
reply
2.3k
views
Answer:
A: Translational bioinformatics in the era of real-time biomedical, health care and
7.3 years ago by
Prash
▴ 180
1
vote
0
replies
4.2k
views
Answer:
Answer: Getting Protein Information from NCBI Gene ID
updated 4 months ago by
Ram
39k • written 8.1 years ago by
Prash
▴ 180
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