Published in PLoS One on November 11, 2009
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Evaluation of alignment algorithms for discovery and identification of pathogens using RNA-Seq. PLoS One (2013) 0.96
New mutations in chronic lymphocytic leukemia identified by target enrichment and deep sequencing. PLoS One (2012) 0.96
CUSHAW3: sensitive and accurate base-space and color-space short-read alignment with hybrid seeding. PLoS One (2014) 0.96
Massively parallel sequencing approaches for characterization of structural variation. Methods Mol Biol (2012) 0.96
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. Mol Autism (2015) 0.95
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Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype. BMC Med Genet (2012) 0.94
Sensitive and fast mapping of di-base encoded reads. Bioinformatics (2011) 0.94
Epigenetic regulation of microRNA genes and the role of miR-34b in cell invasion and motility in human melanoma. PLoS One (2011) 0.94
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SAMQA: error classification and validation of high-throughput sequenced read data. BMC Genomics (2011) 0.92
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Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene. Brain (2013) 0.92
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Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics (2009) 190.94
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Genome sequencing in microfabricated high-density picolitre reactors. Nature (2005) 150.21
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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays. PLoS Genet (2008) 20.38
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