High-throughput single nucleotide variant discovery in E14 mouse embryonic stem cells provides a new reference genome assembly

Genomics

Volumn 104, Issue 2, 2014, Pages 121-127

  Incarnato, Danny ^a,b   Krepelova, Anna ^a   Neri, Francesco ^a  

^a Human Genetics Foundation (HuGeF)   (Italy)

^b UNIVERSITY OF SIENA   (Italy)

Author keywords

E14; ESC; Genome reference; Genotyping; Sequencing; SNV

Indexed keywords

RNA; SPACER DNA;

ANIMAL CELL; ARTICLE; COMPUTER PROGRAM; CPG ISLAND; EMBRYONIC STEM CELL; ENHANCER REGION; EXON; GENE MAPPING; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPING TECHNIQUE; HIGH THROUGHPUT SCREENING; MOLECULAR BIOLOGY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROBABILITY; PROMOTER REGION; REFERENCE DATABASE; RNA SPLICING; SEQUENCE ANALYSIS; SEQUENCE DATABASE; UNTRANSLATED REGION; ANIMAL; CELL LINE; DNA SEQUENCE; FACTUAL DATABASE; GENOME; GENOMICS; HIGH THROUGHPUT SEQUENCING; METABOLISM; PROCEDURES; REGULATORY SEQUENCE; REPRODUCIBILITY; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; CELL LINE; DATABASES, FACTUAL; DNA, INTERGENIC; EMBRYONIC STEM CELLS; GENOME; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; MICE; POLYMORPHISM, SINGLE NUCLEOTIDE; REGULATORY SEQUENCES, NUCLEIC ACID; REPRODUCIBILITY OF RESULTS; SEQUENCE ANALYSIS, DNA;

EID: 84906061645     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/j.ygeno.2014.06.007     Document Type: Article

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