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16 Apr 24 - 17 Apr 24
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DNA library preparation of difficult samples for NGS on Illumina® platforms. Read more...
Optimal sequencing of your cfDNA, FFPE and ChIP DNA Read more...
PCR-free NGS prep with highest library diversity, lowest inputs Read more...
NGS library prep for hybridization capture Read more...
Providing ultimate coverage of methylated DNA. Read more...
DNA library preparation on Ion Torrent platforms Read more...
The Accel-NGS 2S MID Indexing Kits have been designed, optimized, and validated for use withAccel-NGS 2S DNA Library Kits on Illumina platforms, and aid in low frequency variant detection, as well as accurate de-duplication of single read... Read more...
Customizable Targeting of Key Oncology Variants Read more...
Interrogate clinically-relevant colorectal cancer genes Read more...
Sequence key genes implicated in Lynch Syndrome Read more...
Interrogate NSCLC and SCLC genes Read more...
Interrogate hematological malignancy genes Read more...
All-exon sequencing of TP53 Read more...
All-exon profiling of BRCA1 and BRCA2 genes Read more...
Expansive profiling of BRCA1, BRCA2 and PALB2 genes Read more...
Sequence hotspots in EGFR, KRAS, NRAS and BRAF Read more...
Build Your Own Custom Targeted NGS Panel Read more...
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Targeted Sequencing for Cystic Fibrosis Read more...