Context dependence of meiotic recombination hotspots in yeast: the relationship between recombination activity of a reporter construct and base composition.

Por Petes, Thomas D, Merker, Jason D
Publicado em 2002

Next-generation sequencing in hematologic malignancies: what will be the dividends?

Por Merker, Jason D., Valouev, Anton, Gotlib, Jason
Publicado em 2012

Patterns of heteroduplex formation associated with the initiation of meiotic recombination in the yeast Saccharomyces cerevisiae.

Por Merker, Jason D, Dominska, Margaret, Petes, Thomas D
Publicado em 2003

Design and Evaluation of a Real-Time PCR Assay for Quantification of JAK2 V617F and Wild-Type JAK2 Transcript Levels in the Clinical Laboratory

Por Merker, Jason D., Jones, Carol D., Oh, Stephen T., Schrijver, Iris, Gotlib, Jason, Zehnder, James L.
Publicado em 2010

Feasibility of using microbeads with holographic barcodes to track DNA specimens in the clinical molecular laboratory

Por Merker, Jason D., O’Grady, Naomi, Gojenola, Linda, Dao, Mai, Lenta, Ross, Yeakley, Joanne M., Schrijver, Iris
Publicado em 2013

A Balanced Look at the Implications of Genomic (and Other “Omics”) Testing for Disease Diagnosis and Clinical Care

Por Boyd, Scott D., Galli, Stephen J., Schrijver, Iris, Zehnder, James L., Ashley, Euan A., Merker, Jason D.
Publicado em 2014

A genetic approach for identifying critical residues in the fingers and palm subdomains of HIV-1 reverse transcriptase

Por Wrobel, John A., Chao, Shih-Fong, Conrad, Michael J., Merker, Jason D., Swanstrom, Ronald, Pielak, Gary J., Hutchison, Clyde A.
Publicado em 1998

The histone methylase Set2p and the histone deacetylase Rpd3p repress meiotic recombination at the HIS4 meiotic recombination hotspot in Saccharomyces cerevisiae

Por Merker, Jason D., Dominska, Margaret, Greenwell, Patricia W., Rinella, Erica, Bouck, David C, Shibata, Yoichiro, Strahl, Brian D., Mieczkowski, Piotr, Petes, Thomas D.
Publicado em 2008

Diagnosis of a Critical Respiratory Illness Caused by Human Metapneumovirus by Use of a Pan-Virus Microarray

Por Chiu, Charles Y., Alizadeh, Ash A., Rouskin, Silvi, Merker, Jason D., Yeh, Elaine, Yagi, Shigeo, Schnurr, David, Patterson, Bruce K., Ganem, Don, DeRisi, Joseph L.
Publicado em 2007

Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms

Por Oh, Stephen T., Simonds, Erin F., Jones, Carol, Hale, Matthew B., Goltsev, Yury, Gibbs, Kenneth D., Merker, Jason D., Zehnder, James L., Nolan, Garry P., Gotlib, Jason
Publicado em 2010

A study of the mutational landscape of pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma

Por Ozawa, Michael G, Bhaduri, Aparna, Chisholm, Karen M, Baker, Steven A, Ma, Lisa, Zehnder, James L, Luna-Fineman, Sandra, Link, Michael P, Merker, Jason D, Arber, Daniel A, Ohgami, Robert S
Publicado no Mod Pathol (2016)

Measurement and clinical monitoring of human lymphocyte clonality by massively parallel VDJ pyrosequencing

Por Boyd, Scott D., Marshall, Eleanor L., Merker, Jason D., Maniar, Jay M., Zhang, Lyndon N., Sahaf, Bita, Jones, Carol D., Simen, Birgitte B., Hanczaruk, Bozena, Nguyen, Khoa D., Nadeau, Kari C., Egholm, Michael, Miklos, David B., Zehnder, James L., Fire, Andrew Z.
Publicado em 2009

Individual Variation in the Germline Ig Gene Repertoire Inferred from Variable Region Gene Rearrangements

Por Boyd, Scott D., Gaëta, Bruno A., Jackson, Katherine J., Fire, Andrew Z., Marshall, Eleanor L., Merker, Jason D., Maniar, Jay M., Zhang, Lyndon N., Sahaf, Bita, Jones, Carol D., Simen, Birgitte B., Hanczaruk, Bozena, Nguyen, Khoa D., Nadeau, Kari C., Egholm, Michael, Miklos, David B., Zehnder, James L., Collins, Andrew M.
Publicado no J Immunol (2010)

Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

Por Merker, Jason D., Roskin, Krishna M., Ng, Dana, Pan, Cuiping, Fisk, Dianna G., King, Jasmine J., Hoh, Ramona, Stadler, Michael, Okumoto, Lawrence M., Abidi, Parveen, Hewitt, Rhonda, Jones, Carol D., Gojenola, Linda, Clark, Michael J., Zhang, Bing, Cherry, Athena M., George, Tracy I., Snyder, Michael, Boyd, Scott D., Zehnder, James L., Fire, Andrew Z., Gotlib, Jason
Publicado em 2013

Clinical Interpretation and Implications of Whole-Genome Sequencing

Por Dewey, Frederick E., Grove, Megan E., Pan, Cuiping, Goldstein, Benjamin A., Bernstein, Jonathan A., Chaib, Hassan, Merker, Jason D., Goldfeder, Rachel L., Enns, Gregory M., David, Sean P., Pakdaman, Neda, Ormond, Kelly E., Caleshu, Colleen, Kingham, Kerry, Klein, Teri E., Whirl-Carrillo, Michelle, Sakamoto, Kenneth, Wheeler, Matthew T., Butte, Atul J., Ford, James M., Boxer, Linda, Ioannidis, John P. A., Yeung, Alan C., Altman, Russ B., Assimes, Themistocles L., Snyder, Michael, Ashley, Euan A., Quertermous, Thomas
Publicado em 2014

Assuring the quality of next-generation sequencing in clinical laboratory practice

Por Gargis, Amy S, Kalman, Lisa, Berry, Meredith W, Bick, David P, Dimmock, David P, Hambuch, Tina, Lu, Fei, Lyon, Elaine, Voelkerding, Karl V, Zehnbauer, Barbara A, Agarwala, Richa, Bennett, Sarah F, Chen, Bin, Chin, Ephrem L H, Compton, John G, Das, Soma, Farkas, Daniel H, Ferber, Matthew J, Funke, Birgit H, Furtado, Manohar R, Ganova-Raeva, Lilia M, Geigenmüller, Ute, Gunselman, Sandra J, Hegde, Madhuri R, Johnson, Philip L F, Kasarskis, Andrew, Kulkarni, Shashikant, Lenk, Thomas, Liu, C S Jonathan, Manion, Megan, Manolio, Teri A, Mardis, Elaine R, Merker, Jason D, Rajeevan, Mangalathu S, Reese, Martin G, Rehm, Heidi L, Simen, Birgitte B, Yeakley, Joanne M, Zook, Justin M, Lubin, Ira M
Publicado em 2012