
Affiliated with a Castle Connolly Top Hospital
Also known as:
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For detailed information, please contact Dr. Ji's office.
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All Other Third Party
Central California Alliance for Health
Department of Veterans Affairs
Imperial Health Plan (CA)
Managed Care of America
Medicare
Partnership Health Plan
Santa Clara Family Health Plan
Valley Health Plan
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High sensitivity detection and quantitation of D copy number and single nucleotide variants with
Alytical chemistry, 2014
Identification of Insertion Deletion Mutations from Deep Targeted Resequencing.
Jourl of data mining in genomics & proteomics, 2013
DETECTING MUTATIONS IN MIXED SAMPLE SEQUENCING DATA USING EMPIRICAL BAYES
ANLS OF APPLIED STATISTICS, 2012
Performance comparison of whole-genome sequencing platforms
TURE BIOTECHNOLOGY, 2012
Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin
Translatiol medicine (Sunnyvale, Calif.), 2012
Targeted sequencing library preparation by genomic D circularization
BMC BIOTECHNOLOGY, 2011
Efficient targeted resequencing of human germline
TURE BIOTECHNOLOGY, 2011
Genetic-based biomarkers and next-generation sequencing
PERSOLIZED MEDICINE, 2011
Oncogenic BRAF Mutation with CDKN2A Ictivation Is Characteristic of a Subset of Pediatric Malignt
CANCER RESEARCH, 2010
Identification of a biomarker panel using a multiplex proximity ligation
JOURL OF TRANSLATIOL MEDICINE, 2009
Next-generation D sequencing
TURE BIOTECHNOLOGY, 2008
Multigene amplification and massively parallel sequencing for cancer mutation discovery
PROCEEDINGS OF THE TIOL ACADEMY OF SCIENCES OF THE UNITED STATES OF AM, 2007
Multiplexed protein detection by proximity ligation for cancer biomarker validation
TURE METHODS, 2007
Under-expression of Kalirin-7 increases iNOS activity in cultured cells
JOURL OF ALZHEIMERS DISEASE, 2007
Reproducibility Probability Score
TURE BIOTECHNOLOGY, 2006
The MicroArray Quality Control
TURE BIOTECHNOLOGY, 2006
Data quality in genomics and microarrays
TURE BIOTECHNOLOGY, 2006
Molecular inversion probe alysis of gene copy alterations reveals distinct categories of colorectal
CANCER RESEARCH, 2006
A functiol assay for mutations in tumor suppressor genes caused by mismatch repair deficiency
HUMAN MOLECULAR GENETICS, 2001
Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)
AMERICAN JOURL OF MEDICAL GENETICS, 1999
Molecular classification of the inherited hamartoma polyposis syndromes
AMERICAN JOURL OF HUMAN GENETICS, 1998
Inherited mutations in PTEN that are associated with breast cancer, Cowden disease
AMERICAN JOURL OF HUMAN GENETICS, 1997
HOTSPOTS FOR UNSELECTED TY1 TRANSPOSITION EVENTS ON YEAST CHROMOSOME-III ARE NEAR TRANSFER
CELL, 1993
A programmable method for massively parallel targeted sequencing.
Nucleic acids research, 2014
High sensitivity detection and quantitation of DNA copy number and single nucleotide variants
Analytical chemistry, 2014
Systematic genomic identification of colorectal cancer genes delineating advanced from early
BMC MEDICAL GENOMICS, 2013
RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using
BMC research notes, 2013
Identification of Insertion Deletion Mutations from Deep Targeted Resequencing.
Journal of data mining in genomics & proteomics, 2013
DETECTING MUTATIONS IN MIXED SAMPLE SEQUENCING DATA USING EMPIRICAL BAYES
ANNALS OF APPLIED STATISTICS, 2012
Improving bioinformatic pipelines for exome variant calling
GENOME MEDICINE, 2012
Performance comparison of whole-genome sequencing platforms
NATURE BIOTECHNOLOGY, 2012
A cross-sample statistical model for SNP detection in short-read sequencing data
NUCLEIC ACIDS RESEARCH, 2012
Quantitative and Sensitive Detection of Cancer Genome Amplifications from Formalin Fixed Paraffin
Translational medicine (Sunnyvale, Calif.), 2012
Identification of a novel deletion mutant strain in Saccharomyces cerevisiae that results in a
BioDiscovery
Ultrasensitive detection of rare mutations using next-generation targeted resequencing
NUCLEIC ACIDS RESEARCH, 2012
The Human OligoGenome Resource
Nucleic acids research, 2012
Targeted sequencing library preparation by genomic DNA circularization
BMC BIOTECHNOLOGY, 2011
Efficient targeted resequencing of human germline
NATURE BIOTECHNOLOGY, 2011
A Flexible Approach for Highly Multiplexed Candidate Gene Targeted Resequencing
PLOS ONE, 2011
Genetic-based biomarkers and next-generation sequencing
PERSONALIZED MEDICINE, 2011
Oncogenic BRAF Mutation with CDKN2A Inactivation Is Characteristic of a Subset of Pediatric
CANCER RESEARCH, 2010
Detecting simultaneous changepoints in multiple sequences.
Biometrika, 2010
Targeted deep resequencing of the human cancer genome using next-generation technologies
BIOTECHNOLOGY AND GENETIC ENGINEERING REVIEWS, VOL 27, 2010
Identification of a biomarker panel using a multiplex proximity ligation
JOURNAL OF TRANSLATIONAL MEDICINE, 2009
Molecular inversion probes reveal patterns of 9p21 deletion
CANCER GENETICS AND CYTOGENETICS, 2009
Disperse-a software system for design of selector probes for exon resequencing applications
BIOINFORMATICS, 2009
Molecular inversion probe assay for allelic quantitation.
Methods in molecular biology (Clifton, N.J.), 2009
Next-generation DNA sequencing
NATURE BIOTECHNOLOGY, 2008
Multigene amplification and massively parallel sequencing for cancer mutation discovery
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES O, 2007
Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector
NUCLEIC ACIDS RESEARCH, 2007
Multiplexed protein detection by proximity ligation for cancer biomarker validation
NATURE METHODS, 2007
Under-expression of Kalirin-7 increases iNOS activity in cultured cells
JOURNAL OF ALZHEIMERS DISEASE, 2007
Reproducibility Probability Score
NATURE BIOTECHNOLOGY, 2006
The MicroArray Quality Control
NATURE BIOTECHNOLOGY, 2006
Data quality in genomics and microarrays
NATURE BIOTECHNOLOGY, 2006
Molecular inversion probe analysis of gene copy alterations reveals distinct categories of
CANCER RESEARCH, 2006
A functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency
HUMAN MOLECULAR GENETICS, 2001
Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)
AMERICAN JOURNAL OF MEDICAL GENETICS, 1999
Molecular classification of the inherited hamartoma polyposis syndromes
AMERICAN JOURNAL OF HUMAN GENETICS, 1998
Inherited mutations in PTEN that are associated with breast cancer, Cowden disease
AMERICAN JOURNAL OF HUMAN GENETICS, 1997
HOTSPOTS FOR UNSELECTED TY1 TRANSPOSITION EVENTS ON YEAST CHROMOSOME-III ARE NEAR TRANSFER
CELL, 1993
