Synapse.
Mapping the field…

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For students choosing a research topic

Find the open corner of your research field.Research. Mapped. Simplified.Know your field before you commit.Choose a topic that's actually open.Every topic has a gap. Find yours.

See which parts of your topic are crowded and which are still open, mapped from real papers.

See a sample map
  • Real papers from OpenAlex
  • Every paper links to its source
  • Free during early access
A real map in Synapse: “CRISPR gene editing”, 60 papers in five Active subtopics, with one subtopic opened beside the map.

01The problem

Most students pick a topic blind.

The usual check on a topic comes from a supervisor, weeks in. Compare the two timelines.

  1. Week 1Pick a topic that sounds interesting.
  2. Week 4Read everything you can find on it.
  3. Week 10Your supervisor says that corner is already crowded.
  4. Week 11Start again, with less time.

The usual way: weeks of reading before anyone checks the space.

02From papers to a map

Watch 60 papers become a map.

  1. 0160 real papersThe most relevant matches for “CRISPR gene editing”, from OpenAlex.
  2. 02Linked and groupedPapers that cite each other or share distinctive words end up together.
  3. 03Five subtopics, ratedEach is rated by its share of the papers. Here all five are Active; five papers stand alone.
Papers mapped
60
Subtopics
5
Free to read
53
CRISPRCas9 tools13 papers · ActiveTherapies12 papers · ActiveDelivery11 papers · ActiveCrops11 papers · ActiveMultiplex8 papers · Active
A real run, CRISPR gene editing: 60 papers in 5 Active subtopics and 5 single papers. Names are ours; the groups and numbers are the map’s.

03How it works

Three steps. A few minutes.

Type a topic in plain words. Synapse fetches the papers, links them and groups them, then you choose.

See how a map is built
microplastics in soilMap it

Plain words are fine. No keywords or search tricks.

04What you get

Everything you need to choose well.

The map, how crowded each part is, and the real papers behind every read.

Open a real map

05Why you can trust it

Grounded in real papers. Not guesses.

Ask a chatbot for a research gap, then look at what Synapse shows instead.

Example of a typical chatbot answerIs there a research gap in CRISPR delivery?Yes! Delivering CRISPR into plant cells with nanoparticles is a major unexplored gap that researchers haven’t looked at yet.Sources: none shown
  • No papers you can checkNothing to open, read or cite.
  • No idea how crowded it is“Unexplored” with no numbers behind it.
  • Ask again, get another answerThe wording changes, and so can the claim.
Read exactly how a map is built

06Who it’s for

Built for the moment before you commit.

Check your topic first.

Free during early access. A map takes a few minutes.

  1. 2013Nature Protocols

    Genome engineering using the CRISPR-Cas9 system

    12,013 citationsActive

  2. 2016Nature

    Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage

    5,703 citationsOpen

  3. 2013Cell

    One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering

    3,598 citationsActive

  4. 2013Cell

    Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity

    3,411 citationsOpen

07FAQ

Questions, answered.

Still stuck?Email synapsepapers@gmail.com and we’ll help.

Synapse.

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For students choosing a research topic

Find the open corner of your research field.Research. Mapped. Simplified.Know your field before you commit.Choose a topic that's actually open.Every topic has a gap. Find yours.

See which parts of your topic are crowded and which are still open, mapped from real papers.

For the best experience, open Synapse on a desktop.

01The problem

Most students pick a topic blind.

The usual check on a topic comes from a supervisor, weeks in. Compare the two timelines.

  1. Week 1Pick a topic that sounds interesting.
  2. Week 4Read everything you can find on it.
  3. Week 10Your supervisor says that corner is already crowded.
  4. Week 11Start again, with less time.

The usual way: weeks of reading before anyone checks the space.

02From papers to a map

Watch 60 papers become a map.

  1. 0160 real papersThe most relevant matches for “CRISPR gene editing”, from OpenAlex.
  2. 02Linked and groupedPapers that cite each other or share distinctive words end up together.
  3. 03Five subtopics, ratedEach is rated by its share of the papers. Here all five are Active; five papers stand alone.
Papers mapped
60
Subtopics
5
Free to read
53
CRISPRCas9 tools13 papers · ActiveTherapies12 papers · ActiveDelivery11 papers · ActiveCrops11 papers · ActiveMultiplex8 papers · Active
A real run, CRISPR gene editing: 60 papers in 5 Active subtopics and 5 single papers. Names are ours; the groups and numbers are the map’s.

03How it works

Three steps. A few minutes.

Type a topic in plain words. Synapse fetches the papers, links them and groups them, then you choose.

See how a map is built
microplastics in soilMap it

Plain words are fine. No keywords or search tricks.

04What you get

Everything you need to choose well.

The map, how crowded each part is, and the real papers behind every read.

05Why you can trust it

Grounded in real papers. Not guesses.

Ask a chatbot for a research gap, then look at what Synapse shows instead.

Example of a typical chatbot answerIs there a research gap in CRISPR delivery?Yes! Delivering CRISPR into plant cells with nanoparticles is a major unexplored gap that researchers haven’t looked at yet.Sources: none shown
  • No papers you can checkNothing to open, read or cite.
  • No idea how crowded it is“Unexplored” with no numbers behind it.
  • Ask again, get another answerThe wording changes, and so can the claim.
Read exactly how a map is built

06Who it’s for

Built for the moment before you commit.

Check your topic first.

For the best experience, open Synapse on a desktop.

  1. 2013Nature Protocols

    Genome engineering using the CRISPR-Cas9 system

    12,013 citationsActive

  2. 2016Nature

    Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage

    5,703 citationsOpen

  3. 2013Cell

    One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering

    3,598 citationsActive

  4. 2013Cell

    Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity

    3,411 citationsOpen

07FAQ

Questions, answered.

Still stuck?Email synapsepapers@gmail.com and we’ll help.