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rbagnall ♦ 1.4k
Status: New
Handle: @rbagnall4544
Reputation: 1360
Email: r***********@hotmail.com
Joined: 8 months ago
Last seen: 8 months ago
Location: Australia

about me

Comment: C: How do we call this phenomenon in evolution?
0 Votes | 1 Reply
14 months ago
rbagnall
♦ 1.4k
Answer: A: RNA-seq alignment rate is too low.
0 Votes | 1 Reply
15 months ago
rbagnall
♦ 1.4k
Answer: A: Detecting Homozygous Insertion from Sanger Seq
3 Votes | 0 Replies
18 months ago
rbagnall
♦ 1.4k
Comment: C: Find Intersections Between ClinVar Track and VCF In IGV
1 Vote | 1 Reply
19 months ago
rbagnall
♦ 1.4k
Comment: C: Find Intersections Between ClinVar Track and VCF In IGV
1 Vote | 1 Reply
19 months ago
rbagnall
♦ 1.4k
Answer: A: Find Intersections Between ClinVar Track and VCF In IGV
3 Votes | 1 Reply
19 months ago
rbagnall
♦ 1.4k
Comment: C: Update RefSeq database with Ensembl VEP
2 Votes | 0 Replies
21 months ago
rbagnall
♦ 1.4k
Update RefSeq database with Ensembl VEP
4 Votes | 2 Replies
21 months ago
rbagnall
♦ 1.4k
• updated 21 months ago
Emily_Ensembl
18k
Comment: C: How can I deal with this publication issue?
0 Votes | 1 Reply
22 months ago
rbagnall
♦ 1.4k
Answer: A: gnomad_AF from VEP is NA
1 Vote | 1 Reply
22 months ago
rbagnall
♦ 1.4k
Comment: C: snpEff inappropriate interpretation of variants?
0 Votes | 0 Replies
2.6 years ago
rbagnall
♦ 1.4k
Answer: A: snpEff inappropriate interpretation of variants?
2 Votes | 1 Reply
2.6 years ago
rbagnall
♦ 1.4k
Answer: A: Which tool to calculate per site stats on vcf file?
1 Vote | 0 Replies
2.6 years ago
rbagnall
♦ 1.4k
Answer: A: Extracting Codons from a SNP alignment
0 Votes | 0 Replies
2.6 years ago
rbagnall
♦ 1.4k
Answer: A: Human Mitochondrial Variants Annotation
1 Vote | 0 Replies
2.8 years ago
rbagnall
♦ 1.4k
Answer: A: Do People Import VCF Files Into Databases? (2016 version)
1 Vote | 0 Replies
3.4 years ago
rbagnall
♦ 1.4k
Answer: A: Finding variations in mitochondrial genomes
0 Votes | 0 Replies
3.5 years ago
rbagnall
♦ 1.4k
Comment: C: How to extract specific chromosome from vcf file
4 Votes | 2 Replies
3.6 years ago
rbagnall
♦ 1.4k
Comment: C: Number of SNPs captured by targeted sequencing panels
0 Votes | 0 Replies
3.8 years ago
rbagnall
♦ 1.4k
Answer: A: Number of SNPs captured by targeted sequencing panels
1 Vote | 1 Reply
3.8 years ago
rbagnall
♦ 1.4k
Answer: A: Targeted capture sequencing data
1 Vote | 1 Reply
3.8 years ago
rbagnall
♦ 1.4k
Answer: A: Dataset for NGS
0 Votes | 0 Replies
3.9 years ago
rbagnall
♦ 1.4k
Answer: A: sequence head change!
1 Vote | 1 Reply
3.9 years ago
rbagnall
♦ 1.4k
Comment: C: Using VCFTools (v0.1.13) with ExAC (release 0.3.1)
0 Votes | 1 Reply
3.9 years ago
rbagnall
♦ 1.4k
Answer: A: Confusing HGVS notation
4 Votes | 1 Reply
3.9 years ago
rbagnall
♦ 1.4k
Answer: A: Explain bioinformatics to a 10 year old
5 Votes | 1 Reply
4.0 years ago
rbagnall
♦ 1.4k
Comment: C: From gene symbol list to their coordinates
0 Votes | 1 Reply
4.0 years ago
rbagnall
♦ 1.4k
Answer: A: From gene symbol list to their coordinates
0 Votes | 1 Reply
4.0 years ago
rbagnall
♦ 1.4k
Answer: C: (SIFT, Polyphen, PROVEAN) vs. (ANNOVAR) vs. (LOFTEE)
4 Votes | 1 Reply
4.0 years ago
rbagnall
♦ 1.4k
Comment: C: How can I find the most studied SNP of a gene?
0 Votes | 0 Replies
4.1 years ago
rbagnall
♦ 1.4k
Answer: A: How can I find the most studied SNP of a gene?
1 Vote | 3 Replies
4.1 years ago
rbagnall
♦ 1.4k
Comment: C: How to decide how broken a gene is
1 Vote | 0 Replies
4.2 years ago
rbagnall
♦ 1.4k
Comment: C: LOD score of a single genotype
0 Votes | 0 Replies
4.2 years ago
rbagnall
♦ 1.4k
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