TY - GEN
T1 - FASP
T2 - 2016 IEEE 13th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2016
AU - Wang, Yinxue
AU - Shi, Guilai
AU - Miller, David J.
AU - Wang, Yizhi
AU - Broussard, Gerard
AU - Wang, Yue
AU - Tian, Lin
AU - Yu, Guoqiang
N1 - Publisher Copyright:
© 2016 IEEE.
PY - 2016/6/15
Y1 - 2016/6/15
N2 - We propose a machine learning approach to characterize the functional status of astrocytes, the most abundant cells in human brain, based on time-lapse Ca2+ imaging data. The interest in analyzing astrocyte Ca2+ dynamics is evoked by recent discoveries that astrocytes play proactive regulatory roles in neural information processing, and is enabled by recent technical advances in modern microscopy and ultrasensitive genetically encoded Ca2+ indicators. However, current analysis relies on eyeballing the time-lapse imaging data and manually drawing regions of interest, which not only limits the analysis throughput but also at risk to miss important information encoded in the big complex dynamic data. Thus, there is an increased demand to develop sophisticated tools to dissect Ca2+ signaling in astrocytes, which is challenging due to the complex nature of Ca2+ signaling and low signal to noise ratio. We develop Functional AStrocyte Phenotyping (FASP) to automatically detect functionally independent units (FIUs) and extract the corresponding characteristic curves in an integrated way. FASP is data-driven and probabilistically principled, flexibly accounts for complex patterns and accurately controls false discovery rates. We demonstrate the effectiveness of FASP on both synthetic and real data sets.
AB - We propose a machine learning approach to characterize the functional status of astrocytes, the most abundant cells in human brain, based on time-lapse Ca2+ imaging data. The interest in analyzing astrocyte Ca2+ dynamics is evoked by recent discoveries that astrocytes play proactive regulatory roles in neural information processing, and is enabled by recent technical advances in modern microscopy and ultrasensitive genetically encoded Ca2+ indicators. However, current analysis relies on eyeballing the time-lapse imaging data and manually drawing regions of interest, which not only limits the analysis throughput but also at risk to miss important information encoded in the big complex dynamic data. Thus, there is an increased demand to develop sophisticated tools to dissect Ca2+ signaling in astrocytes, which is challenging due to the complex nature of Ca2+ signaling and low signal to noise ratio. We develop Functional AStrocyte Phenotyping (FASP) to automatically detect functionally independent units (FIUs) and extract the corresponding characteristic curves in an integrated way. FASP is data-driven and probabilistically principled, flexibly accounts for complex patterns and accurately controls false discovery rates. We demonstrate the effectiveness of FASP on both synthetic and real data sets.
UR - http://www.scopus.com/inward/record.url?scp=84978370536&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84978370536&partnerID=8YFLogxK
U2 - 10.1109/ISBI.2016.7493281
DO - 10.1109/ISBI.2016.7493281
M3 - Conference contribution
AN - SCOPUS:84978370536
T3 - Proceedings - International Symposium on Biomedical Imaging
SP - 351
EP - 354
BT - 2016 IEEE International Symposium on Biomedical Imaging
PB - IEEE Computer Society
Y2 - 13 April 2016 through 16 April 2016
ER -