Bell JM - Search Results

1

Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy.

Bell JM, Lau BT, Greer SU, Wood-Bouwens C, Xia LC, Connolly ID, Gephart MH, Ji HP. Bell JM, et al. Nucleic Acids Res. 2017 Nov 2;45(19):e162. doi: 10.1093/nar/gkx712. Nucleic Acids Res. 2017. PMID: 28977555 Free PMC article.

2

A flexible approach for highly multiplexed candidate gene targeted resequencing.

Natsoulis G, Bell JM, Xu H, Buenrostro JD, Ordonez H, Grimes S, Newburger D, Jensen M, Zahn JM, Zhang N, Ji HP. Natsoulis G, et al. Among authors: bell jm. PLoS One. 2011;6(6):e21088. doi: 10.1371/journal.pone.0021088. Epub 2011 Jun 30. PLoS One. 2011. PMID: 21738606 Free PMC article.

3

Ultrasensitive detection of rare mutations using next-generation targeted resequencing.

Flaherty P, Natsoulis G, Muralidharan O, Winters M, Buenrostro J, Bell J, Brown S, Holodniy M, Zhang N, Ji HP. Flaherty P, et al. Nucleic Acids Res. 2012 Jan;40(1):e2. doi: 10.1093/nar/gkr861. Epub 2011 Oct 19. Nucleic Acids Res. 2012. PMID: 22013163 Free PMC article.

4

Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing.

Myllykangas S, Buenrostro JD, Natsoulis G, Bell JM, Ji HP. Myllykangas S, et al. Among authors: bell jm. Nat Biotechnol. 2011 Oct 23;29(11):1024-7. doi: 10.1038/nbt.1996. Nat Biotechnol. 2011. PMID: 22020387 Free PMC article.

5

A cross-sample statistical model for SNP detection in short-read sequencing data.

Muralidharan O, Natsoulis G, Bell J, Newburger D, Xu H, Kela I, Ji H, Zhang N. Muralidharan O, et al. Nucleic Acids Res. 2012 Jan;40(1):e5. doi: 10.1093/nar/gkr851. Epub 2011 Nov 7. Nucleic Acids Res. 2012. PMID: 22064853 Free PMC article.

6

The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.

Newburger DE, Natsoulis G, Grimes S, Bell JM, Davis RW, Batzoglou S, Ji HP. Newburger DE, et al. Among authors: bell jm. Nucleic Acids Res. 2012 Jan;40(Database issue):D1137-43. doi: 10.1093/nar/gkr973. Epub 2011 Nov 18. Nucleic Acids Res. 2012. PMID: 22102592 Free PMC article.

7

Targeted sequencing library preparation by genomic DNA circularization.

Myllykangas S, Natsoulis G, Bell JM, Ji HP. Myllykangas S, et al. Among authors: bell jm. BMC Biotechnol. 2011 Dec 14;11:122. doi: 10.1186/1472-6750-11-122. BMC Biotechnol. 2011. PMID: 22168766 Free PMC article.

8

RVD: a command-line program for ultrasensitive rare single nucleotide variant detection using targeted next-generation DNA resequencing.

Cushing A, Flaherty P, Hopmans E, Bell JM, Ji HP. Cushing A, et al. Among authors: bell jm. BMC Res Notes. 2013 May 23;6:206. doi: 10.1186/1756-0500-6-206. BMC Res Notes. 2013. PMID: 23701658 Free PMC article.

9

Identification of Insertion Deletion Mutations from Deep Targeted Resequencing.

Natsoulis G, Zhang N, Welch K, Bell J, Ji HP. Natsoulis G, et al. J Data Mining Genomics Proteomics. 2013 Jul 2;4(3):1000132. doi: 10.4172/2153-0602.1000132. J Data Mining Genomics Proteomics. 2013. PMID: 24511426 Free PMC article.

10

A programmable method for massively parallel targeted sequencing.

Hopmans ES, Natsoulis G, Bell JM, Grimes SM, Sieh W, Ji HP. Hopmans ES, et al. Among authors: bell jm. Nucleic Acids Res. 2014 Jun;42(10):e88. doi: 10.1093/nar/gku282. Epub 2014 Apr 29. Nucleic Acids Res. 2014. PMID: 24782526 Free PMC article.

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