C. Pabón-Peña

发表

Enrichment of sequencing targets from the human genome by solution hybridization

K. Frazer, O. Harismendy, Xiaoyun Wang, 2009, Genome Biology.

Rapid quantification of DNA libraries for next-generation sequencing.

Harini Ravi, Graham Scott, C. Pabón-Peña, 2010, Methods.

Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology

Paul M. Rindler, Ira W. Deveson, S. Cawley, 2021, Nature Biotechnology.

A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency

David P. Kreil, Paweł P. Łabaj, Jeff S. Jasper, 2021, Genome biology.

Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions

Paul M. Rindler, David P. Kreil, Paweł P. Łabaj, 2021, Genome biology.

MammaPrint and BluePrint Molecular Diagnostics using targeted RNA Next-Generation Sequencing technology.

René Bernards, Jiang Chen, Lorenza Mittempergher, 2019, The Journal of molecular diagnostics : JMD.

Assignment1 of STAT1 to human chromosome 2q32 by FISH and radiation hybrids

C. Pabón-Peña, H. Young, B. Haddad, 1999, Cytogenetic and Genome Research.

Characterization of mutations in ATP8B1 associated with hereditary cholestasis

Richard J. Thompson, N. Freimer, L. Pawlikowska, 2004, Hepatology.

Compound microsatellite repeats: practical and theoretical features.

N. Freimer, C. Pabón-Peña, L. Bull, 1999, Genome research.

Overview of the Agilent Technologies SureSelectTM Target Enrichment System

Scott Happe, A. Giuffre, Emily M LeProust, 2011 .

Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing

David P. Kreil, Paweł P. Łabaj, Hagen U. Tilgner, 2024, Scientific data.

Enrichment of sequencing targets from the human genome by solution hybridization

K. Frazer, O. Harismendy, Xiaoyun Wang, 2009, Genome Biology.