Lin MT - Search Results

1

False positives in multiplex PCR-based next-generation sequencing have unique signatures.

McCall CM, Mosier S, Thiess M, Debeljak M, Pallavajjala A, Beierl K, Deak KL, Datto MB, Gocke CD, Lin MT, Eshleman JR. McCall CM, et al. Among authors: lin mt. J Mol Diagn. 2014 Sep;16(5):541-549. doi: 10.1016/j.jmoldx.2014.06.001. Epub 2014 Jul 11. J Mol Diagn. 2014. PMID: 25017478 Free PMC article.

2

A molecular fraction collecting tool for the ABI 310 automated sequencer.

Lin MT, Rich RG, Shipley RF, Hafez MJ, Tseng LH, Murphy KM, Gocke CD, Eshleman JR. Lin MT, et al. J Mol Diagn. 2007 Nov;9(5):598-603. doi: 10.2353/jmoldx.2007.070022. Epub 2007 Oct 4. J Mol Diagn. 2007. PMID: 17916601 Free PMC article.

3

Δ-PCR, A Simple Method to Detect Translocations and Insertion/Deletion Mutations.

Lin MT, Tseng LH, Rich RG, Hafez MJ, Harada S, Murphy KM, Eshleman JR, Gocke CD. Lin MT, et al. J Mol Diagn. 2011 Jan;13(1):85-92. doi: 10.1016/j.jmoldx.2010.11.004. Epub 2010 Dec 23. J Mol Diagn. 2011. PMID: 21227398 Free PMC article.

4

A virtual pyrogram generator to resolve complex pyrosequencing results.

Chen G, Olson MT, O'Neill A, Norris A, Beierl K, Harada S, Debeljak M, Rivera-Roman K, Finley S, Stafford A, Gocke CD, Lin MT, Eshleman JR. Chen G, et al. Among authors: lin mt. J Mol Diagn. 2012 Mar-Apr;14(2):149-59. doi: 10.1016/j.jmoldx.2011.12.001. Epub 2012 Feb 10. J Mol Diagn. 2012. PMID: 22316529 Free PMC article.

5

Clinical validation of KRAS, BRAF, and EGFR mutation detection using next-generation sequencing.

Lin MT, Mosier SL, Thiess M, Beierl KF, Debeljak M, Tseng LH, Chen G, Yegnasubramanian S, Ho H, Cope L, Wheelan SJ, Gocke CD, Eshleman JR. Lin MT, et al. Am J Clin Pathol. 2014 Jun;141(6):856-66. doi: 10.1309/AJCPMWGWGO34EGOD. Am J Clin Pathol. 2014. PMID: 24838331 Free PMC article.

6

Cytosine deamination is a major cause of baseline noise in next-generation sequencing.

Chen G, Mosier S, Gocke CD, Lin MT, Eshleman JR. Chen G, et al. Among authors: lin mt. Mol Diagn Ther. 2014 Oct;18(5):587-93. doi: 10.1007/s40291-014-0115-2. Mol Diagn Ther. 2014. PMID: 25091469 Free PMC article.

7

Haplotype counting by next-generation sequencing for ultrasensitive human DNA detection.

Debeljak M, Freed DN, Welch JA, Haley L, Beierl K, Iglehart BS, Pallavajjala A, Gocke CD, Leffell MS, Lin MT, Pevsner J, Wheelan SJ, Eshleman JR. Debeljak M, et al. Among authors: lin mt. J Mol Diagn. 2014 Sep;16(5):495-503. doi: 10.1016/j.jmoldx.2014.04.003. J Mol Diagn. 2014. PMID: 25132481 Free PMC article.

8

Haplotype Counting for Sensitive Chimerism Testing: Potential for Early Leukemia Relapse Detection.

Debeljak M, Mocci E, Morrison MC, Pallavajjalla A, Beierl K, Amiel M, Noë M, Wood LD, Lin MT, Gocke CD, Klein AP, Fuchs EJ, Jones RJ, Eshleman JR. Debeljak M, et al. Among authors: lin mt. J Mol Diagn. 2017 May;19(3):427-436. doi: 10.1016/j.jmoldx.2017.01.005. J Mol Diagn. 2017. PMID: 28433078 Free PMC article.

9

Optimizing Insertion and Deletion Detection Using Next-Generation Sequencing in the Clinical Laboratory.

Craven KE, Fischer CG, Jiang L, Pallavajjala A, Lin MT, Eshleman JR. Craven KE, et al. Among authors: lin mt. J Mol Diagn. 2022 Dec;24(12):1217-1231. doi: 10.1016/j.jmoldx.2022.08.006. Epub 2022 Sep 24. J Mol Diagn. 2022. PMID: 36162758 Free PMC article.

10

Test Feasibility of Next-Generation Sequencing Assays in Clinical Mutation Detection of Small Biopsy and Fine Needle Aspiration Specimens.

Zheng G, Tsai H, Tseng LH, Illei P, Gocke CD, Eshleman JR, Netto G, Lin MT. Zheng G, et al. Among authors: lin mt. Am J Clin Pathol. 2016 May;145(5):696-702. doi: 10.1093/ajcp/aqw043. Am J Clin Pathol. 2016. PMID: 27247373 Free PMC article.

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