Kristina Giorda

Biochemistry, Genetics and Molecular Biology · Life Sciences

9h-index2.1kcitations32works0.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(13), Molecular Biology Techniques and Applications(11), Genomics and Phylogenetic Studies(7), Genomics and Rare Diseases(7), Gene expression and cancer classification(4)

Publications32 total

Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology
UNC Libraries·2025Open Access
Abstract 6599: A comprehensive benchmark study of multiple library amplification solutions for NGS
Cancer Research·2025
Abstract 2940: A comparative analysis of library preparation technologies for RNA sequencing from FFPE samples
Cancer Research·2024
Abstract 321: Optimized RNA Seq library preparation for fusion calling from FFPE samples
Cancer Research·2024
Abstract 215: A novel enzymatic library preparation workflow that dramatically reduces artifacts associated with damaged FFPE samples
Cancer Research·2023
A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
Genome biology·2021· 58 citedOpen Access
Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
Genome biology·2021· 38 citedOpen Access
Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology
Nature Biotechnology·2021· 252 citedOpen Access
Abstract 1349: Improved human exome sequencing workflow with the most complete coverage
Cancer Research·2020
De novo assembly of the olive fruit fly (Bactrocera oleae) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly
BMC Genomics·2020· 40 citedOpen Access
Additional file 2 of De novo assembly of the olive fruit fly (Bactrocera oleae) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly
Figshare·2020Open Access
Abstract 3520: Detection of low-frequency variants in highly degraded DNA and RNA samples
Molecular and Cellular Biology / Genetics·2019
Abstract 4348: DNA-based fusion detection using a pan-cancer tumor profiling 532-oncogene panel
Cancer Research·2019
Abstract 3520: Detection of low-frequency variants in highly degraded DNA and RNA samples
Cancer Research·2019
Abstract 4348: DNA-based fusion detection using a pan-cancer tumor profiling 532-oncogene panel
Molecular and Cellular Biology / Genetics·2019· 2 cited
<i>De novo</i> genome assembly of the olive fruit fly ( <i>Bactrocera oleae</i> ) developed through a combination of linked-reads and long-read technologies
2018· 3 citedOpen Access
Abstract 418: Highly efficient duplex DNA tagging strategy improves accuracy of detecting ultra-low-frequency mutations through consensus read reconstruction
Cancer Research·2018
Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing
BMC Genomics·2018· 232 citedOpen Access
Abstract 397: Whole genome copy number variation analysis using a SNP-focused targeted sequencing panel for tumor analysis
Cancer Research·2017· 1 cited
Assessing the suitability of NGS panels for clinical sequencing.
PubMed·2017
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Frequent Co-authors

Kevin Lai(11), Michael Schnall-Levin(10), Mirna Jarosz(9), Sofia Kyriazopoulou-Panagiotopoulou(5), Patrick Marks(5), Heather Ordonez(5), Deanna M. Church(5), Binsheng Gong(4), Todd Richmond(4), Zhihong Zhang(4), Natalia Novoradovskaya(4), James C. Willey(4), Rebecca Kusko(4), Guangchun Chen(4), Fujun Qiu(4), Pierre R. Bushel(4), Simon Cawley(4), Scott Happe(4), Nathan Haseley(4), Quan‐Zhen Li(4)