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Comment: C: Amino Acid Change To Genomic Location
updated 4.5 years ago by 43k • written 8.7 years ago by ▴ 210
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22k
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Comment: C: How To Generate A Bibtex File From Pmids
6.2 years ago by Tommy Carstensen ▴ 210
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1
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22k
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Comment: C: How To Generate A Bibtex File From Pmids
6.2 years ago by Tommy Carstensen ▴ 210
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1
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4.5k
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Comment: C: Best RNAseq spliced aligner?
6.8 years ago by Tommy Carstensen ▴ 210
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4.5k
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Comment: C: Best RNAseq spliced aligner?
6.8 years ago by Tommy Carstensen ▴ 210
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4.5k
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Comment: C: Best RNAseq spliced aligner?
6.8 years ago by Tommy Carstensen ▴ 210
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8.2k
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Comment: C: Hera: A new tool for RNA-Seq analysis
6.8 years ago by Tommy Carstensen ▴ 210
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1
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4.5k
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Comment: C: Best RNAseq spliced aligner?
6.8 years ago by Tommy Carstensen ▴ 210
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1
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4.5k
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Comment: C: Best RNAseq spliced aligner?
6.8 years ago by Tommy Carstensen ▴ 210
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1
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13k
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Comment: C: How to get gene name from coordinates using python.
7.0 years ago by Tommy Carstensen ▴ 210
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1
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19k
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Comment: C: Find Out The Genes That Correspond To My Coordinates
7.0 years ago by Tommy Carstensen ▴ 210
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1
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10k
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Comment: C: get build 37 positions from dbSNP rsIDs
7.0 years ago by Tommy Carstensen ▴ 210
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0
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10k
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Comment: C: get build 37 positions from dbSNP rsIDs
7.0 years ago by Tommy Carstensen ▴ 210
0
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0
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10k
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Comment: C: get build 37 positions from dbSNP rsIDs
7.0 years ago by Tommy Carstensen ▴ 210
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6.2k
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Comment: C: Connect Eqtl And Gwas Study
8.0 years ago by Tommy Carstensen ▴ 210
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11k
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Comment: C: Make List Of All Human Gene Ids (Ens, Hgnc, Entrez) To Ease Conversion Of Ids
8.6 years ago by Tommy Carstensen ▴ 210
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11k
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Comment: C: Make List Of All Human Gene Ids (Ens, Hgnc, Entrez) To Ease Conversion Of Ids
8.6 years ago by Tommy Carstensen ▴ 210
1
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11k
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Comment: C: Make List Of All Human Gene Ids (Ens, Hgnc, Entrez) To Ease Conversion Of Ids
8.6 years ago by Tommy Carstensen ▴ 210
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3.5k
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Comment: C: Protein-Protein Interaction After Mutation
8.6 years ago by Tommy Carstensen ▴ 210
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3.2k
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Comment: C: How to extract the peptide sequence centered the amino acid position of protein?
8.7 years ago by Tommy Carstensen ▴ 210
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9.1k
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Comment: C: Is There A Non-Perl Alternative To Accessing Ensembl'S Api?
8.7 years ago by Tommy Carstensen ▴ 210
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3.4k
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Comment: C: web interface for getting rsID in dbSNP of some coordinate?
8.9 years ago by Tommy Carstensen ▴ 210
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3.7k
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Comment: Comment: 1000G high coverage depth of sequencing?
updated 16 months ago by 43k • written 9.0 years ago by ▴ 210
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6.6k
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Comment: Comment: How can I download snp genotype file from 1000 Genome?
updated 2.1 years ago by 43k • written 9.2 years ago by ▴ 210
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4.5k
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Comment: C: Where can I download a list of mtDNA haplogroup mutations?
9.2 years ago by Tommy Carstensen ▴ 210
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22k
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Comment: C: 1000 Genomes Snps' Ancestral Allele
9.2 years ago by Tommy Carstensen ▴ 210
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2.5k
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Comment: Comment: Does build 37 of the human reference genome contain 2.85Gbp?
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 210
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3.7k
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Comment: C: GATK vs more traditional SNP and alignment tools
9.3 years ago by Tommy Carstensen ▴ 210
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1
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6.8k
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Comment: Comment: mitochondrial variant calling
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 210
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0
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6.8k
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Comment: Comment: mitochondrial variant calling
updated 2.1 years ago by 43k • written 9.3 years ago by ▴ 210
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1
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2.6k
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Comment: Comment: list all records in a vcf file?
updated 3.1 years ago by 43k • written 9.5 years ago by ▴ 210
2
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1
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2.6k
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Comment: Comment: list all records in a vcf file?
updated 3.1 years ago by 43k • written 9.5 years ago by ▴ 210
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