Sequencing error correction without a reference genome

por Sleep, Julie A, Schreiber, Andreas W, Baumann, Ute
Publicado 2013

Combined cetuximab and volumetric modulated arc-radiotherapy in advanced recurrent squamous cell carcinoma of the scalp

por Wollina, Uwe, Schreiber, Andreas, Merla, Knut, Haroske, Gunter
Publicado 2011

Bots in software engineering: a systematic mapping study

por Santhanam, Sivasurya, Hecking, Tobias, Schreiber, Andreas, Wagner, Stefan
Publicado 2022

Combining transcriptional datasets using the generalized singular value decomposition

por Schreiber, Andreas W, Shirley, Neil J, Burton, Rachel A, Fincher, Geoffrey B
Publicado 2008

Discovery of barley miRNAs through deep sequencing of short reads

por Schreiber, Andreas W, Shi, Bu-Jun, Huang, Chun-Yuan, Langridge, Peter, Baumann, Ute
Publicado 2011

Hemolysin coregulated protein 1 as a molecular gluing unit for the assembly of nanoparticle hybrid structures

por Pham, Tuan Anh, Schreiber, Andreas, Sturm (née Rosseeva), Elena V, Schiller, Stefan, Cölfen, Helmut
Publicado 2016

Transcriptome-scale homoeolog-specific transcript assemblies of bread wheat

por Schreiber, Andreas W, Hayden, Matthew J, Forrest, Kerrie L, Kong, Stephan L, Langridge, Peter, Baumann, Ute
Publicado 2012

A novel single-cell based method for breast cancer prognosis

por Li, Xiaomei, Liu, Lin, Goodall, Gregory J., Schreiber, Andreas, Xu, Taosheng, Li, Jiuyong, Le, Thuc D.
Publicado 2020

Dynamic Structural Changes and Thermodynamics in Phase Separation Processes of an Intrinsically Disordered–Ordered Protein Model

por Lüdeke, Steffen, Lohner, Philipp, Stühn, Lara G., Betschart, Martin U., Huber, Matthias C., Schreiber, Andreas, Schiller, Stefan M.
Publicado 2021

A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing’s disease

por De Sousa, Sunita M. C., Manavis, Jim, Feng, Jinghua, Wang, Paul, Schreiber, Andreas W., Scott, Hamish S., Torpy, David J.
Publicado 2020

A comparative analysis of algorithms for somatic SNV detection in cancer

por Roberts, Nicola D., Kortschak, R. Daniel, Parker, Wendy T., Schreiber, Andreas W., Branford, Susan, Scott, Hamish S., Glonek, Garique, Adelson, David L.
Publicado 2013

Constitutive ß-Catenin Signaling by the Viral Chemokine Receptor US28

por Langemeijer, Ellen V., Slinger, Erik, de Munnik, Sabrina, Schreiber, Andreas, Maussang, David, Vischer, Henry, Verkaar, Folkert, Leurs, Rob, Siderius, Marco, Smit, Martine J.
Publicado 2012

Comparative transcriptomics in the Triticeae

por Schreiber, Andreas W, Sutton, Tim, Caldo, Rico A, Kalashyan, Elena, Lovell, Ben, Mayo, Gwenda, Muehlbauer, Gary J, Druka, Arnis, Waugh, Robbie, Wise, Roger P, Langridge, Peter, Baumann, Ute
Publicado 2009

Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss

por Venugopal, Parvathy, Gagliardi, Lucia, Forsyth, Cecily, Feng, Jinghua, Phillips, Kerry, Babic, Milena, Poplawski, Nicola K., Rienhoff, Hugh Young, Schreiber, Andreas W., Hahn, Christopher N., Brown, Anna L., Scott, Hamish S.
Publicado 2020

Adjuvant hypofractionated radiotherapy with simultaneous integrated boost after breast-conserving surgery: results of a prospective trial

por Krug, David, Baumann, René, Krockenberger, Katja, Vonthein, Reinhard, Schreiber, Andreas, Boicev, Alexander, Würschmidt, Florian, Weinstrauch, Evelyn, Eilf, Kirsten, Andreas, Peter, Höller, Ulrike, Dinges, Stefan, Piefel, Karen, Zimmer, Jörg, Dellas, Kathrin, Dunst, Jürgen
Publicado 2020

RUNX1 mutations in blast-phase chronic myeloid leukemia associate with distinct phenotypes, transcriptional profiles, and drug responses

por Adnan Awad, Shady, Dufva, Olli, Ianevski, Aleksandr, Ghimire, Bishwa, Koski, Jan, Maliniemi, Pilvi, Thomson, Daniel, Schreiber, Andreas, Heckman, Caroline A., Koskenvesa, Perttu, Korhonen, Matti, Porkka, Kimmo, Branford, Susan, Aittokallio, Tero, Kankainen, Matti, Mustjoki, Satu
Publicado 2020

Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

por De Angelis, Carla, Byrne, Alicia B., Morrow, Rebecca, Feng, Jinghua, Ha, Thuong, Wang, Paul, Schreiber, Andreas W., Babic, Milena, Taranath, Ajay, Manton, Nick, King-Smith, Sarah L., Schwarz, Quenten, Arts, Peer, Scott, Hamish S., Barnett, Christopher
Publicado 2021

Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6

por Byrne, Alicia B., Arts, Peer, Polyak, Steven W., Feng, Jinghua, Schreiber, Andreas W., Kassahn, Karin S., Hahn, Christopher N., Mordaunt, Dylan A., Fletcher, Janice M., Lipsett, Jillian, Bratkovic, Drago, Booker, Grant W., Smith, Nicholas J., Scott, Hamish S.
Publicado 2019

Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome

por Arts, Peer, Garland, Jessica, Byrne, Alicia B., Hardy, Tristan S.E., Babic, Milena, Feng, Jinghua, Wang, Paul, Ha, Thuong, King‐Smith, Sarah L., Schreiber, Andreas W., Crawford, April, Manton, Nick, Moore, Lynette, Barnett, Christopher P., Scott, Hamish S.
Publicado 2020

OR34-6 A Novel Mechanism of SDH-Deficient Tumorigenesis and Implications for Genetic Testing in Patients with Pheochromocytoma-Paraganglioma

por De Sousa, Sunita M.C., Toubia, John, Feng, Jingua, Wang, Paul, Hardy, Tristan S.E., Babic, Milena, Geoghegan, Joel, Hall, Rachel, Scott, Grist, Rawlings, Lesley, Schreiber, Andreas, Luxford, Catherine, Clifton-Bligh, Roderick, Poplawski, Nicola, Scott, Hamish, Torpy, David
Publicado 2019