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How much does it cost to sequence a human genome?

Human genome sequencing cost · $/genome · measured 2001–2022 · fitted live from 22 observations by the Many Minded cost-curve engine.

The last measured value is $525 (2022, OWID / NHGRI). Over the fitted window the series falls 21.5% a year (80% interval −34.3% to −6.2%) — a halving every 2.9 years (80%: 1.7–10.8). Carried forward on that fit, 2027: $156 (80%: $34–$730).

Last measured 2022. The source has not published a newer figure we have verified, so the 4 years since are projections too, not observations.

$525latest measured (2022)−21.5%fitted, per year2.9yper halving22observations, 2001–2022measuredbasis

the curve

human genome sequencing — measured history and fitted projectionhuman genome sequencing: measured 2001–2022 in $/genome, last value $525, fitted at −21.5% a year, projected to 2033 inside an 80% interval. Logarithmic vertical axis.$/genome$10$100$1.00K$10.0K$100K$1.00M$10.0M$100M200120052009201320172021202520292033$525 (2022)
Vertical axis: $/genome, log scale. Solid: measured observations. Dashed: the fitted central projection. Shaded: the 80% interval, which widens with horizon because shocks accumulate.

what this series measures

cost of sequencing one full human genome (NHGRI production cost).

what the fit says

quantityvaluehow it is computed
fitted rate−21.5%/yr (80%: −34.3% to −6.2%)Farmer–Lafond drift over the trailing window · n=11 points, 10 years
halving time2.9 years (80%: 1.7–10.8)implied by the fitted drift
curve checkdecelerating (−61% → −21%/yr)first half of the record versus the second, judged against the direction that helps this metric (falling)
regime break~2009 (−48% → −30%/yr, F=38.5)Chow-style best single breakpoint, kept only above a conservative sup-F threshold

Not shown for this curve, because the machinery returns nothing: Wright's law (no cumulative-deployment series for this technology).

the projection, with its interval

Log cost as a random walk with drift: the forecast variance grows with horizon (τ + τ²/m), which is why these bands widen instead of staying parallel. The middle column is the least useful number on this page; the interval is the claim.

yearcentral fit80% interval
2023$412$228 to $743near horizon
2024$323$135 to $773near horizon
2025$254$84 to $771near horizon
2026$199$53 to $754the band is already wide here
2027$156$34 to $730the band is already wide here
2028$123$21 to $702the band is already wide here
2029$96$14 to $671far horizon — read the interval, not the middle
2030$76$8.95 to $640far horizon — read the interval, not the middle
2031$59$5.80 to $608far horizon — read the interval, not the middle
2032$47$3.77 to $577far horizon — read the interval, not the middle
2033below $45past the point where a number would be theater

The table stops at $45 — a decade below the lowest value ever observed here. Past that, quoting a number would be theater rather than forecast.

questions this page answers

How much does it cost to sequence a human genome?

$525 as of 2022, the latest measured value in the series (OWID / NHGRI). The fitted trend has it falling 21.5% a year, with an 80% interval of −34.3% to −6.2%.

How fast is the cost of sequencing a genome falling?

−21.5% a year over the fitted window, an 80% interval of −34.3% to −6.2% — a halving every 2.9 years (80%: 1.7 to 10.8 years). Fitted from 11 observations spanning 10 years.

What will the cost of sequencing a genome be in 2027?

The central fit says $156, inside an 80% interval of $34 to $730. The interval is the forecast; the middle number is only its midpoint. Bands widen with horizon because shocks accumulate — a constant-width band would be overconfident.

Is the decline in the cost of sequencing a genome accelerating or slowing?

Splitting the record in half, the fitted rate went from −61% to −21% a year — decelerating. A Chow-style test finds a regime break around 2009 (−48% → −30% a year, F=38.5). Regime breaks, not window choice, are what dominate this method's errors — which is why every projection here carries an interval.

Where does this data come from?

OWID / NHGRI. 22 observations spanning 2001–2022. Curated benchmark history, extended by a weekly authoritative fetch and by news figures fact-checked against their source before they may touch a fit. Both the observation ledger and the fitting code are public, and the engine publishes its own calibration score and its misses.

the raw numbers

Every observation behind the fit, unrounded by us and unsmoothed. This table is here on purpose: graphs make people underestimate exponential change, and the raw series beside the curve is the one correction shown to work.

year$/genomechange
2001$95.3M
2002$61.5M−35.5%
2003$40.2M−34.6%
2004$18.5M−53.9%
2005$13.8M−25.5%
2006$10.5M−24.1%
2007$7.15M−31.7%
2008$343K−95.2%
2009$70.3K−79.5%
2010$29.1K−58.6%
2011$7.74K−73.4%
2012$5.90K−23.8%
2013$5.10K−13.6%
2014$4.01K−21.4%
2015$1.25K−68.9%
2016$1.18K−5.5%
2017$1.01K−13.7%
2018$1.23K+21.4%
2019$606−50.8%
2020$512−15.6%
2021$454−11.3%
2022$525+15.5%

where this comes from

Recent briefs from HEALTH, the daily record of what actually moved:

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