TY  - GEN
AU  - Carr,Ian M
AU  - Morgan,Joanne
AU  - Watson,Christopher
AU  - Melnik,Svitlana
AU  - Diggle,Christine P
AU  - Logan,Clare V
AU  - Harrison,Sally M
AU  - Taylor,Graham R
AU  - Pena,Sergio D J
AU  - Markham,Alexander F
AU  - Alkuraya,Fowzan S
AU  - Black,Graeme C M
AU  - Ali,Manir
AU  - Bonthron,David T
TI  - Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data
SN  - 1098-1004
PY  - 2014///0127
KW  - Computational Biology
KW  - methods
KW  - Exome
KW  - genetics
KW  - Genetic Predisposition to Disease
KW  - Genetic Variation
KW  - Genome, Human
KW  - Humans
KW  - Polymorphism, Single Nucleotide
KW  - Sequence Analysis, DNA
KW  - Software
N1  - Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.22322
ER  -