Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - Nature …, 2019 - nature.com
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance,–. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance,–. We …
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis… - Nature …, 2019 - pubmed.ncbi.nlm.nih.gov
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance 1-3. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance 1-3. We …
[引用][C] Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - Nature …, 2019 - cir.nii.ac.jp
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute
leukemia | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
leukemia | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索 …
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia.
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - Nature …, 2019 - europepmc.org
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance 1–3. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance 1–3. We …
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - paper.sciencenet.cn
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance1, 2, 3. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance1, 2, 3. We …
[HTML][HTML] Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis… - Nature …, 2019 - ncbi.nlm.nih.gov
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance 1–3. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance 1–3. We …
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia.
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - Nature …, 2019 - go.gale.com
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance. sup. 1-3 …
phenotypes spanning DNA accessibility, gene expression and protein abundance. sup. 1-3 …
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
JM Granja, S Klemm, LM McGinnis, AS Kathiria… - paper.sciencenet.cn
Identifying the causes of human diseases requires deconvolution of abnormal molecular
phenotypes spanning DNA accessibility, gene expression and protein abundance1, 2, 3. We …
phenotypes spanning DNA accessibility, gene expression and protein abundance1, 2, 3. We …
