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publications [2017/07/25 14:52]
mlabadm [2017]
publications [2017/07/27 15:11] (現在)
mlabadm [2017]
ライン 32: ライン 32:
   -  Yoshizato T, Nannya Y, Atsuta Y, Shiozawa Y, Iijima-Yamashita Y, Yoshida K, Shiraishi Y, Suzuki H, Nagata Y, Sato Y, Kakiuchi N, Matsuo K, Onizuka M, Kataoka K, Chiba K, Tanaka H, Ueno H, Nakagawa MM, Przychodzen B, Haferlach C, Kern W, Aoki K, Itonaga H, Kanda Y, Sekeres MA, Maciejewski JP, Haferlach T, Miyazaki Y, Horibe K, Sanada M, Miyano S, Makishima H, Ogawa S. Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation. Blood. 129(17):2347-2358, 2017. doi: 10.1182/blood-2016-12-754796.   -  Yoshizato T, Nannya Y, Atsuta Y, Shiozawa Y, Iijima-Yamashita Y, Yoshida K, Shiraishi Y, Suzuki H, Nagata Y, Sato Y, Kakiuchi N, Matsuo K, Onizuka M, Kataoka K, Chiba K, Tanaka H, Ueno H, Nakagawa MM, Przychodzen B, Haferlach C, Kern W, Aoki K, Itonaga H, Kanda Y, Sekeres MA, Maciejewski JP, Haferlach T, Miyazaki Y, Horibe K, Sanada M, Miyano S, Makishima H, Ogawa S. Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation. Blood. 129(17):2347-2358, 2017. doi: 10.1182/blood-2016-12-754796.
   -  Zhang YZ, Yamaguchi R, Imoto S, Miyano S. Sequence-specific bias correction for RNA-seq data using recurrent neural networks. BMC Genomics. 18(Suppl 1):1044, 2017. doi: 10.1186/s12864-016-3262-5.   -  Zhang YZ, Yamaguchi R, Imoto S, Miyano S. Sequence-specific bias correction for RNA-seq data using recurrent neural networks. BMC Genomics. 18(Suppl 1):1044, 2017. doi: 10.1186/s12864-016-3262-5.
 +  -  Onuki R, Yamaguchi R, Shibuya T, Kanehisa M, Goto S. Revealing Phenotype-Associated Functional Differences by Genome-Wide Scan of Ancient Haplotype Blocks. PLOS ONE, 12(4): e0176530, 2017.
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publications.txt · 最終更新: 2017/07/27 15:11 by mlabadm