Inventor

CHAN KWAN CHEE

HK88 patents

⚠️ This page may combine multiple inventors who share the name “CHAN KWAN CHEE”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

CHAN KWAN CHEE

UNIV HONG KONG CHINESE

Diagnosing cancer using genomic sequencing

Size-based analysis of fetal or tumor DNA fraction in plasma

Fetal methylation markers

Methylation pattern analysis of tissues in a DNA mixture

Detecting genetic aberrations associated with cancer using genomic sequencing

Analysis of fragmentation patterns of cell-free DNA

Detection of genetic or molecular aberrations associated with cancer

Size-based analysis of cell-free tumor DNA for classifying level of cancer

Non-invasive determination of methylome of tumor from plasma

Classification of cancer level based on genomic coordinates of outermost nucleotides of cell-free DNA

Non-invasive determination of methylome of fetus or tumor from plasma

Maternal plasma transcriptome analysis by massively parallel RNA sequencing

Detecting mutations for cancer screening

Determination of the depth coverage of the fetal genome

Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

Determining percentage of fetal DNA in maternal sample

Determining progress of chromosomal aberrations over time

Analysis of fragmentation patterns of cell-free DNA

Analysis of fragmentation patterns of cell-free DNA

Analysis of fragmentation patterns of cell-free DNA

Using nucleic acid size range for noninvasive cancer detection

Using size and number aberrations in plasma DNA for detecting cancer

Size-based genomic analysis

Non-invasive determination of type of cancer

Size-based analysis of fetal DNA fraction in plasma

Enhancement of cancer screening using cell-free viral nucleic acids

Non-invasive determination of methylome of tumor from plasma

Determining a nucleic acid sequence imbalance using multiple markers

Determination of base modifications of nucleic acids

Molecular analyses using long cell-free fragments in pregnancy

Identifying a de novo fetal mutation from a maternal biological sample

Using nucleic acid size range for noninvasive cancer detection

Accurate deduction of fetal DNA fraction with shallow-depth sequencing of maternal plasma

Detecting chromosomal aberrations associated with cancer using genomic sequencing

LO YUK MING DENNIS

Fetal genomic analysis from a maternal biological sample

Size-based genomic analysis

Detection of genetic or molecular aberrations associated with cancer

Methods for detecting fetal DNA in a plasma or serum sample from a pregnant woman

Noninvasive prenatal genotyping of fetal sex chromosomes

Diagnosing fetal chromosomal aneuploidy using genomic sequencing

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing

LO YUK-MING DENNIS

Determining a nucleic acid sequence imbalance

Diagnosing fetal chromosomal aneuploidy using paired end

Fetal methylation markers

THE CHINESE UNIV OF HONG KONG OFFICE OF RESEARCH AND KNOWLEDGE TRANSFER SERVICES

Diagnostic applications using nucleic acid fragments