Evidence map›Paper›PMID 38495703›Full record

ArticleBiomedical optics express2024

Towards ultrafast quantitative phase imaging via differentiable microscopy [Invited].

Udith Haputhanthri, Kithmini Herath, Ramith Hettiarachchi, Hasindu Kariyawasam, Azeem Ahmad, Balpreet S Ahluwalia, Ganesh Acharya, Chamira U S Edussooriya, Dushan N Wadduwage

Abstract read
In one paragraph

Article in Biomedical optics express, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Udith HaputhanthriCenter for Advanced Imaging, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.
Kithmini HerathCenter for Advanced Imaging, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.
Ramith HettiarachchiCenter for Advanced Imaging, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.
Hasindu KariyawasamCenter for Advanced Imaging, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.
Azeem AhmadDepartment of Physics and Technology, UiT The Arctic University of Norway, Tromsø, 9037, Norway.ORCID https://orcid.org/0000-0001-5372-1571
Balpreet S AhluwaliaDepartment of Physics and Technology, UiT The Arctic University of Norway, Tromsø, 9037, Norway.ORCID https://orcid.org/0000-0001-7841-6952
Ganesh AcharyaDivision of Obstetrics and Gynecology, Department of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
Chamira U S EdussooriyaDepartment of Electronic and Telecommunication Engineering, University of Moratuwa, Sri Lanka.
Dushan N WadduwageCenter for Advanced Imaging, Faculty of Arts and Sciences, Harvard University, Cambridge, MA 02138, USA.

Funding

Structured light temporal focusing depth-resolved wide-field FLIM-FRET for in vivo synaptic imagingR21MH130067 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI NEDIVI, ELLY, SO, PETER T. · 2022 to 2023
$451k
NIMH NIH HHS R21 MH130067
6 · The paper itself

Abstract

With applications ranging from metabolomics to histopathology, quantitative phase microscopy (QPM) is a powerful label-free imaging modality. Despite significant advances in fast multiplexed imaging sensors and deep-learning-based inverse solvers, the throughput of QPM is currently limited by the pixel-rate of the image sensors. Complementarily, to improve throughput further, here we propose to acquire images in a compressed form so that more information can be transferred beyond the existing hardware bottleneck of the image sensor. To this end, we present a numerical simulation of a learnable optical compression-decompression framework that learns content-specific features. The proposed differentiable quantitative phase microscopy (∂-QPM) first uses learnable optical processors as image compressors. The intensity representations produced by these optical processors are then captured by the imaging sensor. Finally, a reconstruction network running on a computer decompresses the QPM images post aquisition. In numerical experiments, the proposed system achieves compression of × 64 while maintaining the SSIM of ∼0.90 and PSNR of ∼30 dB on cells. The results demonstrated by our experiments open up a new pathway to QPM systems that may provide unprecedented throughput improvements.

Identifiers

PMID38495703
PMCPMC10942716

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.