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Fiona Hyland

science applications international corporation (saic)

36H指数
215论文数
2.9W被引数
收录论文 51
发表时间
A comprehensive genomic profiling of myeloid malignancies demonstrates mutational spectrum of DNA variants, FLT3-ITDs, and gene fusions
err2024-03-22
err0
PREAI
errHuang, Jiajie; Gu, Haigang; Orton, Janet; Sedova, Marina; Rozenzhak, Sophie; Hyland, Fiona; Liu, Guang
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MetFlow: Automated nextflow pipeline for Ion AmpliSeq methylation assay designs
err2024-03-22
err0
PREAI
errBedre, Renesh; Kaul, Drishti; Sharma, Anupma; Hatch, Andrew; Pickle, Loni; Li, Na; Hyland, Fiona
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Validation of a Targeted Next-Generation Sequencing Panel for Tumor Mutation Burden Analysis Results from the Onconetwork Immuno-Oncology Consortium
err2021-07-01
err2
errOAAI
errFenizia, Francesca; Alborelli, Ilaria; Costa, Jose Luis; Vollbrecht, Claudia; Bellosillo, Beatriz; Dinjens, Winand; Endris, Volker; Heydt, Carina; Leonards, Katharina; Merkelback-Bruse, Sabine; Pfarr, Nicole; van Marion, Ronald; Allen, Christopher; Chaudhary, Ruchi; Gottimukkala, Rajesh; Hyland, Fiona; Wong-Ho, Elaine; Jermann, Philip; Machado, Jose Carlos; Hummel, Michael; Stenzinger, Albrecht; Normanno, Nicola
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AUTOMATED ION TORRENT BASED SOLUTION ENABLES ACCURATE GUT MICROBIOME QUANTIFICATION OF BACTERIAL SPECIES RELEVANT TO RESEARCH IN CANCER AND ITS RESPONSE TO IMMUNOTHERAPY
err2020-12-10
err0
errOAAI
errSarda, Shrutii; Merrill, David; Shin, Heesun; McGeachy, Anna; Drews, Birgit; Lee, Wing; Gottimukkala, Rajesh; Au-Young, Janice; Hyland, Fiona
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Next generation sequencing assay for detection of gene fusions and exon deletion events in tissue and liquid biopsy samples at very low frequency
err2020-08-15
err0
PREAI
errGottimukkala, Rajesh K.; Hyland, Fiona C.; Marcovitz, Amir; Schageman, Jeoffrey; Bagai, Varun; Cao, Ru; Williams, Paul D.; Myrand, Scott P.; Gu, Jian; Sadis, Seth; Bramlett, Kelli S.
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RNA sequencing based gene fusion detection with oncomine comprehensive assay plus
err2020-08-15
err0
PREAI
errMarcovitz, Amir; Gottimukkala, Rajesh K.; Bee, Gary G.; Kilzer, Jennifer M.; Mital, Vinay K.; Wong-Ho, Elain; Yang, Chenchen; Tseng, Yu-Ting; Myrand, Scott P.; Williams, Paul D.; Sadis, Seth; Hyland, Fiona C.
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A novel system that produces pre-qualified cancer NGS panels with customizable content
err2020-08-15
err0
PREAI
errRoman, Steven; Scafe, Charles; Zhu, Yun; Farfan, Fernando; McKnight, Brooke; Bandla, Santoshi; Yang, Chenchen; Tseng, Yu-Ting; Duan, Xiaoping; Patel, Jigar; Arksey, Natasha; Sadis, Seth; Hyland, Fiona
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Automated TRB locus haplotype analysis by long-amplicon TCRB chain sequencing for immune-related adverse events biomarker research
err2020-08-15
err0
PREAI
errBurke, Jennifer; Chan, Frances; Huang, Jiajie; Sedova, Marina; Looney, Timothy; Hyland, Fiona
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Development and analytical validation of a novel next-generation DNA sequencing assay, the oncomine lymphoma panel, to detect SNV, insertion, deletion and copy number variants in 25 Lymphoma genes in FFPE samples
err2020-08-15
err0
PREAI
errHyland, Fiona; Scafe, Charles; Zhu, Yun; Yang, Chenchen; Tseng, Yu-Ting; McKnight, Brooke; Farfan, Fernando; Bandla, Santhoshi; Sadis, Seth; Roman, Steve
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Custom primer design pipeline and analysis workflow for targeted methylation sequencing using NGS Ion AmpliSeq technology
err2020-08-15
err3
PREAI
errLuo, Zunping; Pickle, Loni; Hatch, Andrew; Ewing, Aren; Hyland, Fiona; Berman, David; Patel, Palak; Andersen, Mark
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Clonal lineage and somatic hypermutation analysis of chronic lymphocytic leukemia by long-amplicon IGH chain sequencing
err2020-08-15
err0
PREAI
errChang, Jayde; Davis, Zadie; Quest, Graeme; Feilloter, Harriet; Toro, Michelle; Lowman, Geoffrey; Pickle, Loni; Hyland, Fiona; Looney, Timothy
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Custom next-generation sequencing primer designs for targeted sequencing of multi strain viral targets
err2020-08-15
err0
PREAI
errSingh, Ratnesh; Li, Na; Luo, Zunping; McGeachy, Anna; Alcantara, Antonio F. Martinez; Ewing, Aren; Hyland, Fiona C.
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Development of customizable targeted RNA fusion panels using a novel automated high-multiplexing primer design strategy
err2020-08-15
err0
PREAI
errLi, Na; Martinez-Alcantara, Antonio; Ewing, Aren; Gottimukkala, Rajesh; Hyland, Fiona; Sadis, Seth
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Comparative analysis of RNA versus DNA as input material for IGH repertoire sequencing based detection of rare clonal B cells at a frequency of 10E-6
err2020-08-15
err0
PREAI
errToro, Michelle; Pickle, Loni; Chang, Jayde; Looney, Timothy; Lowman, Geoffrey; Andersen, Mark; Hyland, Fiona
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Improvement of tumor mutation burden measurement by removal of deaminated bases in FFPE DNA
err2019-07-01
err1
PREAI
errTom, Warren; Chaudhary, Ruchi; Mittal, Vinay; Cyanam, Dinesh; Casuga, Iris; Wong-Ho, Elaine; Bennett, Rob; Hyland, Fiona; Sadis, Seth; Au-Young, Janice
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Assessing tumor mutational burden and profiling variants from FFPE samples using a PCR-based next-generation sequencing assay
err2019-07-01
err0
PREAI
errChaudhary, Ruchi; Scafe, Charles; Cyanam, Dinesh; Mittal, Vinay; Tom, Warren; Au-Young, Janice; Sadis, Seth; Hyland, Fiona
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A scalable solution for tumor mutational burden from formalinfixed, paraffin-embedded samples using the Oncomine Tumor Mutation Load Assay
err2018-12-01
err35
errOAAI
errChaudhary, Ruchi; Quagliata, Luca; Martin, Jermann Philip; Alborelli, Ilaria; Cyanam, Dinesh; Mittal, Vinay; Tom, Warren; Au-Young, Janice; Sadis, Seth; Hyland, Fiona
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