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Author

Nick Van Helleputte

Other affiliations: IMEC
Bio: Nick Van Helleputte is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Signal & Artifact (error). The author has an hindex of 22, co-authored 74 publications receiving 1670 citations. Previous affiliations of Nick Van Helleputte include IMEC.


Papers
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Journal ArticleDOI
TL;DR: This paper presents a MUlti-SEnsor biomedical IC (MUSEIC), which features a high-performance, low-power analog front-end (AFE) and fully integrated DSP achieving 10 × or more energy savings in vector multiply-accumulate executions.
Abstract: This paper presents a MUlti-SEnsor biomedical IC (MUSEIC). It features a high-performance, low-power analog front-end (AFE) and fully integrated DSP. The AFE has three biopotential readouts, one bio-impedance readout, and support for general-purpose analog sensors The biopotential readout channels can handle large differential electrode offsets ( ${\pm} $ 400 mV), achieve high input impedance ( ${>}$ 500 M $\Omega$ ), low noise ( ${ 620 nVrms in 150 Hz), and large CMRR ( ${>}$ 110 dB) without relying on trimming while consuming only 31 $\mu$ W/channel. In addition, fully integrated real-time motion artifact reduction, based on simultaneous electrode-tissue impedance measurement, with feedback to the analog domain is supported. The bio-impedance readout with pseudo-sine current generator achieves a resolution of 9.8 m $\Omega$ / $\surd$ Hz while consuming just 58 $\mu$ W/channel. The DSP has a general purpose ARM Cortex M0 processor and an HW accelerator optimized for energy-efficient execution of various biomedical signal processing algorithms achieving 10 $\times$ or more energy savings in vector multiply-accumulate executions.

193 citations

Journal ArticleDOI
TL;DR: This paper describes a mixed-signal ECG System-on-Chip (SoC) that is capable of implementing configurable functionality with low-power consumption for portable ECG monitoring applications and can be reduced significantly.
Abstract: This paper describes a mixed-signal ECG System-on-Chip (SoC) that is capable of implementing configurable functionality with low-power consumption for portable ECG monitoring applications. A low-voltage and high performance analog front-end extracts 3-channel ECG signals and single channel electrode-tissue-impedance (ETI) measurement with high signal quality. This can be used to evaluate the quality of the ECG measurement and to filter motion artifacts. A custom digital signal processor consisting of 4-way SIMD processor provides the configurability and advanced functionality like motion artifact removal and R peak detection. A built-in 12-bit analog-to-digital converter (ADC) is capable of adaptive sampling achieving a compression ratio of up to 7, and loop buffer integration reduces the power consumption for on-chip memory access. The SoC is implemented in 0.18 $\mu$ m CMOS process and consumes 32 $\mu$ W from a 1.2 V while heart beat detection application is running, and integrated in a wireless ECG monitoring system with Bluetooth protocol. Thanks to the ECG SoC, the overall system power consumption can be reduced significantly.

193 citations

Journal ArticleDOI
TL;DR: A novel deep learning framework (CorNET) to efficiently estimate heart rate (HR) information and perform biometric identification (BId) using only a wrist-worn, single-channel PPG signal collected in ambulant environment is presented.
Abstract: Advancements in wireless sensor network technologies have enabled the proliferation of miniaturized body-worn sensors, capable of long-term pervasive biomedical signal monitoring. Remote cardiovascular monitoring has been one of the beneficiaries of this development, resulting in non-invasive, photoplethysmography (PPG) sensors being used in ambulatory settings. Wrist-worn PPG, although a popular alternative to electrocardiogram, suffers from motion artifacts inherent in daily life. Hence, in this paper, we present a novel deep learning framework (CorNET) to efficiently estimate heart rate (HR) information and perform biometric identification (BId) using only a wrist-worn, single-channel PPG signal collected in ambulant environment. We have formulated a completely personalized data-driven approach, using a four-layer deep neural network. Two convolution neural network layers are used in conjunction with two long short-term memory layers, followed by a dense output layer for modeling the temporal sequence inherent within the pulsatile signal representative of cardiac activity. The final dense layer is customized with respect to the application, functioning as: regression layer—having a single neuron to predict HR; classification layer—two neurons that identify a subject among a group. The proposed network was evaluated on the TROIKA dataset having 22 PPG records collected during various physical activities. We achieve a mean absolute error of 1.47 ± 3.37 beats per minute for HR estimation and an average accuracy of 96% for BId on 20 subjects. CorNET was further evaluated successfully in an ambulant use-case scenario with custom sensors for two subjects.

163 citations

Journal ArticleDOI
TL;DR: A 384-channel configurable neural probe for large-scale in vivo recording of neural signals and results show a total input-referred noise of 6.4%, dual-band recording and a 171.6 Mbps digital interface.
Abstract: In vivo recording of neural action-potential and local-field-potential signals requires the use of high-resolution penetrating probes. Several international initiatives to better understand the brain are driving technology efforts towards maximizing the number of recording sites while minimizing the neural probe dimensions. We designed and fabricated (0.13- $\mu$ m SOI Al CMOS) a 384-channel configurable neural probe for large-scale in vivo recording of neural signals. Up to 966 selectable active electrodes were integrated along an implantable shank (70 $\mu$ m wide, 10 mm long, 20 $\mu$ m thick), achieving a crosstalk of $-\text{64.4}$ dB. The probe base (5 $\times$ 9 mm $^2$ ) implements dual-band recording and a 171.6 Mbps digital interface. Measurement results show a total input-referred noise of 6.4 $\mu$ V $_{\mathrm{rms}}$ and a total power consumption of 49.1 $\mu$ W/channel.

139 citations

Journal ArticleDOI
TL;DR: A comprehensive review of state-of-the-art research on heart rate estimation from wrist-worn PPG signals and brief theoretical details about PPG sensing and other potential applications–biometric identification, disease diagnosis using wrist PPG are presented.
Abstract: Photoplethysmography (PPG) is a low-cost, non-invasive, and optical technique used to detect blood volume changes in the microvascular tissue bed, measured from the skin surface. It has traditionally been used in commercial medical devices for oxygen saturation, blood pressure monitoring, and cardiac activity for assessing peripheral vascular disease and autonomic function. There has been a growing interest to incorporate PPG sensors in daily life, capable of use in ambulatory settings. However, inferring cardiac information (e.g. heart rate) from PPG traces in such situations is extremely challenging, because of interferences caused by motion. Following the IEEE Signal Processing Cup in 2015, numerous methods have been proposed for estimating particularly the average heart rate using wrist-worn PPG during physical activity. Details on PPG technology, sensor development, and applications have been well documented in the literature. Hence, in this paper, we have presented a comprehensive review of state-of-the-art research on heart rate estimation from wrist-worn PPG signals. Our review also encompasses brief theoretical details about PPG sensing and other potential applications–biometric identification, disease diagnosis using wrist PPG. This paper will set a platform for future research on pervasive monitoring using wrist PPG.

138 citations


Cited by
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Journal ArticleDOI
08 Nov 2017-Nature
TL;DR: The fully integrated functionality and small size of Neuropixels probes allowed large populations of neurons from several brain structures to be recorded in freely moving animals and opens a path towards recording of brain-wide neural activity during behaviour.
Abstract: New silicon probes known as Neuropixels are shown to record from hundreds of neurons simultaneously in awake and freely moving rodents. Sensory, motor and cognitive operations involve the coordinated action of large neuronal populations across multiple brain regions. Existing technologies reliably measure activity from a relatively small number of neurons with high spatial and temporal resolution, or from a large volume of neurons with low resolution. Timothy Harris and colleagues describe the design, fabrication and performance of Neuropixels, a silicon probe that can measure well-isolated neural activity from hundreds of neurons. They integrated these probes into a lightweight system that could record activity simultaneously and with high fidelity from hundreds of neurons in awake and freely moving rodents. Sensory, motor and cognitive operations involve the coordinated action of large neuronal populations across multiple brain regions in both superficial and deep structures1,2. Existing extracellular probes record neural activity with excellent spatial and temporal (sub-millisecond) resolution, but from only a few dozen neurons per shank. Optical Ca2+ imaging3,4,5 offers more coverage but lacks the temporal resolution needed to distinguish individual spikes reliably and does not measure local field potentials. Until now, no technology compatible with use in unrestrained animals has combined high spatiotemporal resolution with large volume coverage. Here we design, fabricate and test a new silicon probe known as Neuropixels to meet this need. Each probe has 384 recording channels that can programmably address 960 complementary metal–oxide–semiconductor (CMOS) processing-compatible low-impedance TiN6 sites that tile a single 10-mm long, 70 × 20-μm cross-section shank. The 6 × 9-mm probe base is fabricated with the shank on a single chip. Voltage signals are filtered, amplified, multiplexed and digitized on the base, allowing the direct transmission of noise-free digital data from the probe. The combination of dense recording sites and high channel count yielded well-isolated spiking activity from hundreds of neurons per probe implanted in mice and rats. Using two probes, more than 700 well-isolated single neurons were recorded simultaneously from five brain structures in an awake mouse. The fully integrated functionality and small size of Neuropixels probes allowed large populations of neurons from several brain structures to be recorded in freely moving animals. This combination of high-performance electrode technology and scalable chip fabrication methods opens a path towards recording of brain-wide neural activity during behaviour.

1,443 citations

Journal ArticleDOI
12 Jan 2017-Sensors
TL;DR: This paper has presented and compared several low-cost and non-invasive health and activity monitoring systems that were reported in recent years and compatibility of several communication technologies as well as future perspectives and research challenges in remote monitoring systems will be discussed.
Abstract: Life expectancy in most countries has been increasing continually over the several few decades thanks to significant improvements in medicine, public health, as well as personal and environmental hygiene. However, increased life expectancy combined with falling birth rates are expected to engender a large aging demographic in the near future that would impose significant burdens on the socio-economic structure of these countries. Therefore, it is essential to develop cost-effective, easy-to-use systems for the sake of elderly healthcare and well-being. Remote health monitoring, based on non-invasive and wearable sensors, actuators and modern communication and information technologies offers an efficient and cost-effective solution that allows the elderly to continue to live in their comfortable home environment instead of expensive healthcare facilities. These systems will also allow healthcare personnel to monitor important physiological signs of their patients in real time, assess health conditions and provide feedback from distant facilities. In this paper, we have presented and compared several low-cost and non-invasive health and activity monitoring systems that were reported in recent years. A survey on textile-based sensors that can potentially be used in wearable systems is also presented. Finally, compatibility of several communication technologies as well as future perspectives and research challenges in remote monitoring systems will be discussed.

795 citations

Journal ArticleDOI
TL;DR: The focus then turns to the most difficult barrier to potential in vivo use of CRISPR/Cas9, delivery, and detail the various cargos and delivery vehicles reported for CRISpr/ Cas9, including physical delivery vehicles, viral delivery methods, and non-viral delivery methods.
Abstract: Gene therapy has long held promise to correct a variety of human diseases and defects. Discovery of the Clustered Regularly-Interspaced Short Palindromic Repeats (CRISPR), the mechanism of the CRISPR-based prokaryotic adaptive immune system (CRISPR-associated system, Cas), and its repurposing into a potent gene editing tool has revolutionized the field of molecular biology and generated excitement for new and improved gene therapies. Additionally, the simplicity and flexibility of the CRISPR/Cas9 site-specific nuclease system has led to its widespread use in many biological research areas including development of model cell lines, discovering mechanisms of disease, identifying disease targets, development of transgene animals and plants, and transcriptional modulation. In this review, we present the brief history and basic mechanisms of the CRISPR/Cas9 system and its predecessors (ZFNs and TALENs), lessons learned from past human gene therapy efforts, and recent modifications of CRISPR/Cas9 to provide functions beyond gene editing. We introduce several factors that influence CRISPR/Cas9 efficacy which must be addressed before effective in vivo human gene therapy can be realized. The focus then turns to the most difficult barrier to potential in vivo use of CRISPR/Cas9, delivery. We detail the various cargos and delivery vehicles reported for CRISPR/Cas9, including physical delivery methods (e.g. microinjection; electroporation), viral delivery methods (e.g. adeno-associated virus (AAV); full-sized adenovirus and lentivirus), and non-viral delivery methods (e.g. liposomes; polyplexes; gold particles), and discuss their relative merits. We also examine several technologies that, while not currently reported for CRISPR/Cas9 delivery, appear to have promise in this field. The therapeutic potential of CRISPR/Cas9 is vast and will only increase as the technology and its delivery improves.

688 citations