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We find the most relevant new papers for your research and deliver them to your inbox. Every paper is scored against your research profile and evaluated on relevance, methods, novelty, and evidence.

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How It Works

You describe your research once. The most relevant new papers arrive in your inbox with a note explaining why each one matters. Here’s what happens in between.

From Thousands to the Few That Matter

Each stage narrows the field with increasing precision.

Thousands of new papers

Across all disciplines

Six queries, four databases

Tailored to your profile

0 candidates

Merged and deduplicated

Scored to your profile

Every candidate ranked

Scientific evaluation

Four-dimension rubric

Your digest

Each paper explained

Step 1

It Starts With You

You describe your research once: the question you’re asking, the methods you use, the constraints you face. From that description, we build a structured profile of your work and what matters to you.

That profile generates search queries across six categories, from your core domain to adjacent fields that might hold a technique or insight you haven’t seen yet. Each query is shaped for the database it targets.

Your Research

“Investigating LRRK2 kinase inhibition as a therapeutic target for Parkinson’s disease using iPSC-derived dopaminergic neurons and mitochondrial functional assays...”

Generated Queries

DomainLRRK2 kinase inhibitor Parkinson dopaminergic
MethodiPSC dopaminergic neuron differentiation protocol
MechanismLRRK2 mitochondrial dysfunction neurodegeneration
Toolkinase activity assay live-cell imaging neurons
Adjacentalpha-synuclein aggregation lysosomal pathway
Broadneuroprotective small molecule clinical translation
Step 2

Four Sources. Broader Coverage.

Your queries run against four independent academic databases simultaneously. Each covers different corners of the literature. Together, they catch what any single source would miss.

Semantic Scholar

Allen Institute’s citation graph. 200M+ papers with full citation context and metadata.

200M+ papers

OpenAlex

The broadest open academic index. Covers non-English journals, emerging fields, and interdisciplinary work.

250M+ works

arXiv

Preprints indexed hours after submission. Physics, CS, math, and biology before journal publication.

2.4M+ preprints

PubMed

NCBI’s gold standard for biomedical literature. Activated automatically for life science projects.

36M+ articles

Merge & Deduplicate

Results are deduplicated across all four sources. Papers found by multiple databases get a stronger signal.

Step 3

Every Paper Read Against Your Research

Search engines rank papers by their own algorithms. Useful, but generic. A cross-encoder reads your full research description alongside each paper’s abstract in a single pass, scoring how precisely the two relate. Papers are collected across a rolling two-week window to account for indexing delays. Every candidate gets scored. The top papers advance to final evaluation.

Traditional Search

12 results from one database

Our Approach

Found across 4 databases

Step 4

Structured Scientific Evaluation

Relevance alone isn’t enough. A paper can be on your topic but incremental, or use interesting methods but lack evidence.

A language model reads each finalist alongside your interest profile and evaluates it on four dimensions that reflect how researchers actually assess papers. Review articles are detected and filtered based on your preferences. The highest-scoring papers are selected for your digest.

For each paper you receive, the model writes a two-sentence note explaining exactly why it matters to your work. Not a generic summary, but a targeted explanation connecting the paper’s findings to your hypotheses, methods, or goals.

Scientific Rubric

LRRK2 Inhibition Restores Mitochondrial Function in iPSC-Derived Parkinson Neurons

Cell Stem Cell · Feb 2026

Topical Relevance9
Methodological Transfer8
Novelty8
Evidence Strength6

Relevance Note

Why this matters to you

“Demonstrated that LRRK2 kinase inhibition rescues mitochondrial membrane potential and complex I activity in iPSC-derived neurons. The dose-response data and mitochondrial assay approach directly inform the researcher’s experimental design.”

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