Improving bioinformatic pipelines for exome variant calling

por Ji, Hanlee P
Publicado 2012

Single molecule counting and assessment of random molecular tagging errors with transposable giga-scale error-correcting barcodes

por Lau, Billy T., Ji, Hanlee P.
Publicado 2017

MendeLIMS: a web-based laboratory information management system for clinical genome sequencing

por Grimes, Susan M, Ji, Hanlee P
Publicado 2014

Systematic genomic identification of colorectal cancer genes delineating advanced from early clinical stage and metastasis

por Lee, HoJoon, Flaherty, Patrick, Ji, Hanlee P
Publicado 2013

High Sensitivity Detection and Quantitation of DNA Copy Number and Single Nucleotide Variants with Single Color Droplet Digital PCR

por Miotke, Laura, Lau, Billy T., Rumma, Rowza T., Ji, Hanlee P.
Publicado 2014

Correction to High Sensitivity Detection and Quantitation of DNA Copy Number and Single Nucleotide Variants with Single Color Droplet Digital PCR

por Miotke, Laura, Lau, Billy T., Rumma, Rowza T., Ji, Hanlee P.
Publicado 2014

Correction to High Sensitivity Detection and Quantitation of DNA Copy Number and Single Nucleotide Variants with Single Color Droplet Digital PCR

por Miotke, Laura, Lau, Billy T., Rumma, Rowza T., Ji, Hanlee P.
Publicado 2015

Targeted sequencing library preparation by genomic DNA circularization

por Myllykangas, Samuel, Natsoulis, Georges, Bell, John M, Ji, Hanlee P
Publicado 2011

Identification of Insertion Deletion Mutations from Deep Targeted Resequencing

por Natsoulis, Georges, Zhang, Nancy, Welch, Katrina, Bell, John, Ji, Hanlee P
Publicado 2013

The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical–genomic driver associations

por Lee, HoJoon, Palm, Jennifer, Grimes, Susan M., Ji, Hanlee P.
Publicado 2015

Precision Oncology Strategy in Trastuzumab-Resistant Human Epidermal Growth Factor Receptor 2–Positive Colon Cancer: Case Report of Durable Response to Ado-Trastuzumab Emtansine

por Haslem, Derrick S., Ji, Hanlee P., Ford, James M., Nadauld, Lincoln D.
Publicado 2017

RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing

por Cushing, Anna, Flaherty, Patrick, Hopmans, Erik, Bell, John M, Ji, Hanlee P
Publicado 2013

CRISPRpic: fast and precise analysis for CRISPR-induced mutations via prefixed index counting

por Lee, HoJoon, Chang, Howard Y, Cho, Seung Woo, Ji, Hanlee P
Publicado 2020

A functional CRISPR/Cas9 screen identifies kinases that modulate FGFR inhibitor response in gastric cancer

por Chen, Jiamin, Bell, John, Lau, Billy T., Whittaker, Tyler, Stapleton, Darren, Ji, Hanlee P.
Publicado 2019

scPred: accurate supervised method for cell-type classification from single-cell RNA-seq data

por Alquicira-Hernandez, Jose, Sathe, Anuja, Ji, Hanlee P., Nguyen, Quan, Powell, Joseph E.
Publicado 2019

Unique k-mer sequences for validating cancer-related substitution, insertion and deletion mutations

por Lee, HoJoon, Shuaibi, Ahmed, Bell, John M, Pavlichin, Dmitri S, Ji, Hanlee P
Publicado 2020

Allele-specific copy number profiling by next-generation DNA sequencing

por Chen, Hao, Bell, John M., Zavala, Nicolas A., Ji, Hanlee P., Zhang, Nancy R.
Publicado 2015

Single-Color Digital PCR Provides High-Performance Detection of Cancer Mutations from Circulating DNA

por Wood-Bouwens, Christina, Lau, Billy T., Handy, Christine M., Lee, HoJoon, Ji, Hanlee P.
Publicado 2017

Single-cell characterization of CRISPR-modified transcript isoforms with nanopore sequencing

por Kim, Heon Seok, Grimes, Susan M., Hooker, Anna C., Lau, Billy T., Ji, Hanlee P.
Publicado 2021

Magnetic DNA random access memory with nanopore readouts and exponentially-scaled combinatorial addressing

por Lau, Billy, Chandak, Shubham, Roy, Sharmili, Tatwawadi, Kedar, Wootters, Mary, Weissman, Tsachy, Ji, Hanlee P.
Publicado 2023