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2.3k
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Answer: A: How can you explain the high rate of substitution for single branch of BEAST tre
9.6 years ago by DG 7.3k
1
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0
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13k
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Comment: C: FreeBayes vs GATK's HaplotypeCaller
9.7 years ago by DG 7.3k
3
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0
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13k
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Answer: A: FreeBayes vs GATK's HaplotypeCaller
9.7 years ago by DG 7.3k
17
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10
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16k
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Checking kinship coefficients and relationships and comparing genotyping data to exomes
pedigree SNP QC kinship vcf
updated 3.7 years ago by 45k • written 11.1 years ago by 7.3k
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3.8k
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Comment: C: What could be the reason for having mutations in too many cancer samples?
9.7 years ago by DG 7.3k
1
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1
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3.8k
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Comment: C: What could be the reason for having mutations in too many cancer samples?
9.7 years ago by DG 7.3k
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1
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3.8k
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Comment: C: What could be the reason for having mutations in too many cancer samples?
9.7 years ago by DG 7.3k
4
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1
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5.1k
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Answer: A: Should a Bioinformatics PhD student compulsorily conduct wet-lab techniques for
9.7 years ago by DG 7.3k
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4.5k
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Comment: C: Wolfram mathematica in bioinformatic.
9.7 years ago by DG 7.3k
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4.5k
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Answer: A: Wolfram mathematica in bioinformatic.
9.7 years ago by DG 7.3k
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9.1k
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Comment: C: Identifying FLT3-ITD with Pindel
9.7 years ago by DG 7.3k
5
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21
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9.1k
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Identifying FLT3-ITD with Pindel
pindel flt3 tandem duplication ngs SV
updated 3.0 years ago by 45k • written 10.0 years ago by 7.3k
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3.8k
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Comment: C: Opposite genotype filtering in multisample vcf for 2 population
9.7 years ago by DG 7.3k
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3.2k
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Answer: A: How to find the amino acid residue that is encoded by codon which is encoded by
9.7 years ago by DG 7.3k
0
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1
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3.2k
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Answer: A: Looking for open visualization problems in bioinformatics
9.7 years ago by DG 7.3k
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1
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5.6k
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Comment: C: Blastn without nt database
9.7 years ago by DG 7.3k
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1
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5.6k
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Comment: C: Blastn without nt database
9.7 years ago by DG 7.3k
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0
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4.6k
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Answer: A: Merging illumina paired-end data Lxxx and R1/R2
9.7 years ago by DG 7.3k
3
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0
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1.4k
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Answer: A: Performance of Ingenuity variant analysis compared with open source tools like A
9.7 years ago by DG 7.3k
1
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1
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5.6k
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Comment: C: Blastn without nt database
9.7 years ago by DG 7.3k
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1.7k
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Answer: A: RNAseq Analysis of Samples from Multiple Ancestries
9.7 years ago by DG 7.3k
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0
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10k
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Comment: C: Minimum requirements for a laptop for RNA-seq
9.7 years ago by DG 7.3k
2
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1
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10k
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Answer: A: Minimum requirements for a laptop for RNA-seq
9.7 years ago by DG 7.3k
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0
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12k
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Comment: C: Tools To Identify Compound Heterozygous Variants?
9.7 years ago by DG 7.3k
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1
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9.3k
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Comment: C: Can anyone help me with normal-only calling for panel of normals(PON) with MuTec
9.7 years ago by DG 7.3k
1
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2.6k
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Answer: A: Is there any aging-related gene expression database for human?
9.7 years ago by DG 7.3k
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9.3k
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Comment: C: Can anyone help me with normal-only calling for panel of normals(PON) with MuTec
9.7 years ago by DG 7.3k
1
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0
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4.0k
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Answer: A: GWAS for rare diseases?
9.7 years ago by DG 7.3k
2
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1
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9.3k
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Answer: A: Can anyone help me with normal-only calling for panel of normals(PON) with MuTec
9.7 years ago by DG 7.3k
1
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1
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9.3k
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Comment: C: Can anyone help me with normal-only calling for panel of normals(PON) with MuTec
9.7 years ago by DG 7.3k
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0
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9.3k
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Comment: C: Can anyone help me with normal-only calling for panel of normals(PON) with MuTec
9.7 years ago by DG 7.3k
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0
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3.4k
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Comment: C: MuTect Seems to Miss a Lot of Mutations
9.7 years ago by DG 7.3k
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0
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3.4k
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Comment: C: MuTect Seems to Miss a Lot of Mutations
9.7 years ago by DG 7.3k
0
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1
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3.4k
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Comment: C: MuTect Seems to Miss a Lot of Mutations
9.7 years ago by DG 7.3k
0
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1
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3.4k
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Comment: C: MuTect Seems to Miss a Lot of Mutations
9.7 years ago by DG 7.3k
0
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0
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6.9k
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Comment: C: Difference Between SNP and Single Point Mutation in Cancer
9.7 years ago by DG 7.3k
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6.9k
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Comment: C: Difference Between SNP and Single Point Mutation in Cancer
9.7 years ago by DG 7.3k
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0
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6.9k
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Comment: C: Difference Between SNP and Single Point Mutation in Cancer
9.7 years ago by DG 7.3k
0
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1
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6.9k
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Comment: C: Difference Between SNP and Single Point Mutation in Cancer
9.7 years ago by DG 7.3k
0
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0
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4.1k
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Comment: C: Open source All vs All Blast script?
9.8 years ago by DG 7.3k
0
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1
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4.9k
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Comment: C: Cufferge IOError: Errno 2 no such file or directory
9.8 years ago by DG 7.3k
0
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0
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1.9k
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Answer: A: Agilent Haloplex Custom Panel
9.8 years ago by DG 7.3k
1
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0
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3.2k
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Answer: A: Did dbSNP not get the memo about hg38 chromosome names?
9.8 years ago by DG 7.3k
0
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0
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2.2k
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Answer: A: -nan for FPKM value in Cuffdiff output
9.8 years ago by DG 7.3k
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5.9k
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Comment: C: Advice for undergraduate bioinformatics learners
9.8 years ago by DG 7.3k
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5.9k
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Comment: C: Advice for undergraduate bioinformatics learners
9.8 years ago by DG 7.3k
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5.9k
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Comment: C: Advice for undergraduate bioinformatics learners
9.8 years ago by DG 7.3k
2
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1
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5.9k
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Comment: C: Advice for undergraduate bioinformatics learners
9.8 years ago by DG 7.3k
0
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0
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3.3k
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Comment: C: Authoritative genomic regions for Promoter and Enhancer of Human genome
9.8 years ago by DG 7.3k
1
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0
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3.2k
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Comment: C: Are these samples de-multiplexed?
9.8 years ago by DG 7.3k
833 results • Page 7 of 17
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